510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K981907Substantially Equivalent

V.f.i.-Viscous Fluid Infusion Tubing Set

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

K981907 is the FDA 510(k) clearance record for V.F.I.-VISCOUS FLUID INFUSION TUBING SET, a class II device, cleared for Peregrine Surgical , Ltd. on under FDA product code MRH (Pump, Infusion, Ophthalmic). FDA records list 20 510(k) clearances for Peregrine Surgical , Ltd., from to . As of , FDA records show no recalls naming K981907.

Clearance record

Decision date
Received
(64 days to decision)
Product code
MRH Pump, Infusion, Ophthalmic
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
Peregrine Surgical , Ltd. 4050 D Skyron Dr., Doylestown PA
510(k) summary
Summary
Third party review
No

Clearances, product code MRH

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