';


Title 21 Part 886 → Subpart B → §886.1140

Title 21 → Chapter I → Subchapter H → Part 886 → Subpart B → §886.1140

Electronic Code of Federal Regulations e-CFR

Title 21 Part 886 → Subpart B → §886.1140

e-CFR data is current as of September 16, 2019

Title 21Chapter ISubchapter HPart 886Subpart B → §886.1140


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


§886.1140   Ophthalmic chair.

(a) Identification. An ophthalmic chair is an AC-powered or manual device with adjustable positioning in which a patient is to sit or recline during ophthalmological examination or treatment.

(b) Classification. Class I. The AC-powered device and the manual device are exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in §886.9. The manual 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.

[55 FR 48441, Nov. 20, 1990, as amended at 59 FR 63012, Dec. 7, 1994; 66 FR 38810, July 25, 2001]