510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K990518Substantially Equivalent

Peregrine Wet Set, Model Pd400.00

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

K990518 is the FDA 510(k) clearance record for PEREGRINE WET SET, MODEL PD400.00, a class II device, cleared for Peregrine Surgical , Ltd. on under FDA product code FRN (Pump, Infusion). FDA records list 20 510(k) clearances for Peregrine Surgical , Ltd., from to . As of , FDA records show no recalls naming K990518.

Clearance record

Decision date
Received
(35 days to decision)
Product code
FRN Pump, Infusion
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 FRN

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