FDA 510(k) clearance · back to tracker

KARICKHOFF DIAGNOSTIC/LASER LENS

Ocular Instruments, Inc. cleared K862692 on 1986-08-21, decision: substantially equivalent

K-number

K862692

Sponsor

Ocular Instruments, Inc.

Device

KARICKHOFF DIAGNOSTIC/LASER LENS

Class

Class I

Decision

Substantially Equivalent

Decision date

1986-08-21

Product code

HKS

Advisory committee

Ophthalmic

Medical specialty

Ophthalmic

Regulation number

886.1660

Official FDA record

Open K862692on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

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Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.