510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K981741Substantially Equivalent

Carriazo Barraquer Microkeratome

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

K981741 is the FDA 510(k) clearance record for CARRIAZO BARRAQUER MICROKERATOME, a class I device, cleared for Moria, Inc. on under FDA product code HMY (Keratome, Battery-Powered). FDA records list 9 510(k) clearances for Moria, Inc., from to . As of , FDA records show no recalls naming K981741.

Clearance record

Decision date
Received
(67 days to decision)
Product code
HMY Keratome, Battery-Powered
Regulation
21 CFR 886.4370
Device class
Class I
Review panel
Ophthalmic
Applicant
Moria, Inc. 15 Rue Georges Besse, Antony, FR
510(k) summary
Summary
Third party review
No

Clearances, product code HMY

Trailing 12 months

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

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