Cleared Traditional

K894295 - ASTRO-MED ASC-951 PRESSURE PROCESSOR

K894295 is the FDA 510(k) clearance for ASTRO-MED ASC-951 PRESSURE PROCESSOR by Astro-Med, Inc.. It is a Class 2 Cardiovascular device (product code DRQ) cleared through the Traditional 510(k) pathway after a 209-day FDA review.

K894295 · Astro-Med, Inc. · Cardiovascular device
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Jan 1990
Decision
209d
Days
Class 2
Risk

K894295 is an FDA 510(k) clearance for the ASTRO-MED ASC-951 PRESSURE PROCESSOR. Classified as Amplifier And Signal Conditioner, Transducer Signal (product code DRQ), Class II - Special Controls.

Submitted by Astro-Med, Inc. (West Warwick, US). The FDA issued a Cleared decision on January 18, 1990 after a review of 209 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2060 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Astro-Med, Inc. devices

Submission Details

510(k) Number K894295 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 23, 1989
Decision Date January 18, 1990
Days to Decision 209 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
84d slower than avg
Panel avg: 125d · This submission: 209d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DRQ Amplifier And Signal Conditioner, Transducer Signal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2060
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Peers - DRQ Amplifier And Signal Conditioner, Transducer Signal

All 13
Devices cleared under the same product code (DRQ) and FDA review panel - the closest regulatory comparables to K894295.
SIEMENS MEDICAL INFROMATION BUS (MIB II) PROTOCOL CONVERTER
K020277 · Siemens Medical Solutions USA, Inc. · Feb 2002
SIEMENS MEDICAL INFORMATION BUS (MIB II) PROTOCOL CONVERTER
K010640 · Siemens Medical Solutions USA, Inc. · Mar 2001
BARD BIOPOTENTIAL AMPLIFIER II
K901358 · C.R. Bard, Inc. · May 1990
SENTRON PRESSURE MEASURING CATH/PRESSURE INTERFACE
K864320 · Cordis Corp. · Feb 1987
EXTERNAL VALVE FUNCTION BLOCK
K830914 · Honeywell, Inc. · Aug 1983
TRANSDUCER DOME, CAT.#SD-101
K802961 · Sorensen Research · Dec 1980