510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K860332Substantially Equivalent

Diamond Blade Micrometer Knife

Med-Tech Develoment Corp., Clearwater FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K860332 is the FDA 510(k) clearance record for DIAMOND BLADE MICROMETER KNIFE, a class I device, cleared for Med-Tech Develoment Corp. on under FDA product code HNN (Knife, Ophthalmic). FDA records list 5 510(k) clearances for Med-Tech Develoment Corp., from to . As of , FDA records show no recalls naming K860332.

Clearance record

Decision date
Received
(15 days to decision)
Product code
HNN Knife, Ophthalmic
Regulation
21 CFR 886.4350
Device class
Class I
Review panel
Ophthalmic
Applicant
Med-Tech Develoment Corp. 11300 49th St. N., Clearwater FL
Third party review
No

Clearances, product code HNN

Trailing 12 months

FDA records hold no clearances under product code HNN in the trailing twelve months.

FDA records show no clearances under product code HNN in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HNN, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260