';


Title 21 Part 886 → Subpart E → §886.4230

Title 21 → Chapter I → Subchapter H → Part 886 → Subpart E → §886.4230

Electronic Code of Federal Regulations e-CFR

Title 21 Part 886 → Subpart E → §886.4230

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

Title 21Chapter ISubchapter HPart 886Subpart E → §886.4230


Title 21: Food and Drugs
PART 886—OPHTHALMIC DEVICES
Subpart E—Surgical Devices


§886.4230   Ophthalmic knife test drum.

(a) Identification. An ophthalmic knife test drum is a device intended to test the keenness of ophthalmic surgical knives to determine whether resharpening is needed.

(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 35606, Sept. 14, 1988; 66 FR 38813, July 25, 2001]