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Title 21 Part 880 → Subpart F → §880.5270

Title 21 → Chapter I → Subchapter H → Part 880 → Subpart F → §880.5270

Electronic Code of Federal Regulations e-CFR

Title 21 Part 880 → Subpart F → §880.5270

e-CFR data is current as of June 24, 2019

Title 21Chapter ISubchapter HPart 880Subpart F → §880.5270


Title 21: Food and Drugs
PART 880—GENERAL HOSPITAL AND PERSONAL USE DEVICES
Subpart F—General Hospital and Personal Use Therapeutic Devices


§880.5270   Neonatal eye pad.

(a) Identification. A neonatal eye pad is an opaque device used to cover and protect the eye of an infant during therapeutic procedures, such as phototherapy.

(b) Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to §880.9. If the device is not labeled or otherwise represented as sterile, it is exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of §820.180 of this chapter, with respect to general requirements concerning records, and §820.198 of this chapter, with respect to complaint files.

[45 FR 69682, Oct. 21, 1980, as amended at 65 FR 2318, Jan. 14, 2000]