510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K922552Substantially Equivalent

Morse(r) Angiographic Catheters

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

K922552 is the FDA 510(k) clearance record for MORSE(R) ANGIOGRAPHIC CATHETERS, a class II device, cleared for North American Instrument Corp. on under FDA product code DQO (Catheter, Intravascular, Diagnostic). FDA records list 28 510(k) clearances for North American Instrument Corp., from to . As of , FDA records show no recalls naming K922552.

Clearance record

Decision date
Received
(278 days to decision)
Product code
DQO Catheter, Intravascular, Diagnostic
Regulation
21 CFR 870.1200
Device class
Class II
Review panel
Cardiovascular
Applicant
North American Instrument Corp.
510(k) summary
Statement
Third party review
No

Clearances, product code DQO

Trailing 12 months
3 clearances under product code DQO 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 DQO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20261
June 20261
July 20260
August 20260
September 20260
October 20260