510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K980924Substantially Equivalent

Plancon Microlamellar Keratome Evolution

Plancon Instruments, Antony, FR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K980924 is the FDA 510(k) clearance record for PLANCON MICROLAMELLAR KERATOME EVOLUTION, a class I device, cleared for Plancon Instruments on under FDA product code HNO (Keratome, Ac-Powered). FDA records list 3 510(k) clearances for Plancon Instruments, from to . As of , FDA records show no recalls naming K980924.

Clearance record

Decision date
Received
(35 days to decision)
Product code
HNO Keratome, Ac-Powered
Regulation
21 CFR 886.4370
Device class
Class I
Review panel
Ophthalmic
Applicant
Plancon Instruments 15 Rue Georges Besse, Antony, FR
510(k) summary
Summary
Third party review
No

Clearances, product code HNO

Trailing 12 months

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

FDA records show no clearances under product code HNO in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HNO, 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