510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K955554Substantially Equivalent

Hemo-Valve

North American Instrument Corp., Glens Falls NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K955554 is the FDA 510(k) clearance record for HEMO-VALVE, a class II device, cleared for North American Instrument Corp. on under FDA product code DTL (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass). FDA records list 28 510(k) clearances for North American Instrument Corp., from to . As of , FDA records show no recalls naming K955554.

Clearance record

Decision date
Received
(90 days to decision)
Product code
DTL Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
Regulation
21 CFR 870.4290
Device class
Class II
Review panel
Cardiovascular
Applicant
North American Instrument Corp. Pruyns Island Rd., Glens Falls NY
510(k) summary
Summary
Third party review
No

Clearances, product code DTL

Trailing 12 months

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

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