510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K902472Substantially Equivalent

Morse Dt Manifold

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

K902472 is the FDA 510(k) clearance record for MORSE DT MANIFOLD, a class II device, cleared for North American Instrument Corp. on under FDA product code DRS (Transducer, Blood-Pressure, Extravascular). FDA records list 28 510(k) clearances for North American Instrument Corp., from to . As of , FDA records show 2 recalls naming K902472.

Clearance record

Decision date
Received
(80 days to decision)
Product code
DRS Transducer, Blood-Pressure, Extravascular
Regulation
21 CFR 870.2850
Device class
Class II
Review panel
Cardiovascular
Applicant
North American Instrument Corp.
Third party review
No

Clearances, product code DRS

Trailing 12 months
1 clearance under product code DRS in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DRS, 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 20261
October 20260