510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K894295Substantially Equivalent

Astro-Med Asc-951 Pressure Processor

Astro-Med, Inc., West Warwick RI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K894295 is the FDA 510(k) clearance record for ASTRO-MED ASC-951 PRESSURE PROCESSOR, a class II device, cleared for Astro-Med, Inc. on under FDA product code DRQ (Amplifier And Signal Conditioner, Transducer Signal). FDA records list 13 510(k) clearances for Astro-Med, Inc., from to . As of , FDA records show no recalls naming K894295.

Clearance record

Decision date
Received
(209 days to decision)
Product code
DRQ Amplifier And Signal Conditioner, Transducer Signal
Regulation
21 CFR 870.2060
Device class
Class II
Review panel
Cardiovascular
Applicant
Astro-Med, Inc. 600 E. Greenwich Ave., West Warwick RI
Third party review
No

Clearances, product code DRQ

Trailing 12 months

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

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