';


Title 21 Part 886 → Subpart B → §886.1320

Title 21 → Chapter I → Subchapter H → Part 886 → Subpart B → §886.1320

Electronic Code of Federal Regulations e-CFR

Title 21 Part 886 → Subpart B → §886.1320

e-CFR data is current as of September 12, 2019

Title 21Chapter ISubchapter HPart 886Subpart B → §886.1320


Title 21: Food and Drugs
PART 886—OPHTHALMIC DEVICES
Subpart B—Diagnostic Devices


§886.1320   Fornixscope.

(a) Identification. A fornixscope is a device intended to pull back and hold open the eyelid to aid examination of the conjunctiva.

(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 the limitations in §886.9. The device is also 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, with respect to general requirements concerning records, and §820.198, with respect to complaint files.

[52 FR 33355, Sept. 2, 1987, as amended at 53 FR 35604, Sept. 14, 1988; 66 FR 38810, July 25, 2001]