510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K940393Substantially Equivalent

Peregrine Wide Angle Light Pipe

Peregrine Surgical, LLC., Doylestown PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K940393 is the FDA 510(k) clearance record for PEREGRINE WIDE ANGLE LIGHT PIPE, a class II device, cleared for Peregrine Surgical , Ltd. on under FDA product code HJM (Transilluminator, Ac-Powered). FDA records list 20 510(k) clearances for Peregrine Surgical , Ltd., from to . As of , FDA records show one recall naming K940393.

Clearance record

Decision date
Received
(219 days to decision)
Product code
HJM Transilluminator, Ac-Powered
Regulation
21 CFR 886.1945
Device class
Class II
Review panel
Ophthalmic
Applicant
Peregrine Surgical , Ltd. 73 Old Dublin Pike, Doylestown PA
510(k) summary
Statement
Third party review
No

Clearances, product code HJM

Trailing 12 months

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

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