---
kind: "section"
citation: "21 C.F.R. § 880.6050"
title: "21"
number: "880.6050"
heading: "Ice bag."
url: "https://uscodex.org/cfr/21/880.6050"
---

# §880.6050. Ice bag.

- (a) **Identification.** An ice bag is a device intended for medical purposes that is in the form of a container intended to be filled with ice that is used to apply dry cold therapy to an area of the body. The device may include a holder that keeps the bag in place against an external area of the patient.
- (b) **Classification.** Class I (general controls). The device is exempt from the premarket notification procedures in [subpart E of part 807](/cfr/21/part807-subpartE.md) of this chapter, subject to the limitations in [§ 880.9](/cfr/21/880.9.md). If the device is not labeled or otherwise represented as sterile, it is also exempt from the current good manufacturing practice requirements of the quality management system regulation in [part 820](/cfr/21/part820.md) of this chapter, except for requirements concerning records and complaint files under [§ 820.35](/cfr/21/820.35.md) of this chapter.

## Notes

### Amendments

[45 FR 69682, Oct. 21, 1980, as amended at 66 FR 38805, July 25, 2001; 90 FR 55987, Dec. 4, 2025]

### Authority

Authority: 21 U.S.C. 351, 360, 360c, 360e, 360j, 360 l, 371.

### Source

Source: 45 FR 69682, Oct. 21, 1980, unless otherwise noted.

### Amendments

[45 FR 69682, Oct. 21, 1980, as amended at 66 FR 38805, July 25, 2001; 90 FR 55987, Dec. 4, 2025]