510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K973064Substantially Equivalent

Keeler Tearscope-Plus

Keeler Instruments, Inc., Broomall PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K973064 is the FDA 510(k) clearance record for KEELER TEARSCOPE-PLUS, a class II device, cleared for Keeler Instruments, Inc. on under FDA product code HJO (Biomicroscope, Slit-Lamp, Ac-Powered). FDA records list 60 510(k) clearances for Keeler Instruments, Inc., from to . As of , FDA records show no recalls naming K973064.

Clearance record

Decision date
Received
(232 days to decision)
Product code
HJO Biomicroscope, Slit-Lamp, Ac-Powered
Regulation
21 CFR 886.1850
Device class
Class II
Review panel
Ophthalmic
Applicant
Keeler Instruments, Inc. 456 Pkwy., Broomall PA
510(k) summary
Statement
Third party review
No

Clearances, product code HJO

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