510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K061768Substantially Equivalent

Mp-1 Microperimeter

Nidek Technologies SRL, Albignasego (Padova), IT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K061768 is the FDA 510(k) clearance record for MP-1 MICROPERIMETER, a class II device, cleared for Nidek Technologies Srl on under FDA product code HKI (Camera, Ophthalmic, Ac-Powered). FDA records list 5 510(k) clearances for Nidek Technologies Srl, from to . As of , FDA records show no recalls naming K061768.

Clearance record

Decision date
Received
(97 days to decision)
Product code
HKI Camera, Ophthalmic, Ac-Powered
Regulation
21 CFR 886.1120
Device class
Class II
Review panel
Ophthalmic
Applicant
Nidek Technologies Srl Via Dell Artigianato, 6/A, Albignasego (Padova), IT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HKI

Trailing 12 months
3 clearances under product code HKI in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HKI, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260