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FDA 510(k)

ASTRO-MED ASC-951 PRESSURE PROCESSOR

K-Number: K894295 · 1990-01-18

ApplicantAstro-Med, Inc.
Decision Date1990-01-18
Product CodeDRQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ASTRO-MED ASC-951 PRESSURE PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Astro-Med, Inc.. It received FDA 510(k) clearance on 1990-01-18 under 510(k) number K894295. The device is classified under product code DRQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASTRO-MED ASC-951 PRESSURE PROCESSOR?

ASTRO-MED ASC-951 PRESSURE PROCESSOR is a medical device that received FDA 510(k) clearance on 1990-01-18. The listed applicant is Astro-Med, Inc.. The 510(k) number is K894295.

When did ASTRO-MED ASC-951 PRESSURE PROCESSOR receive FDA 510(k) clearance?

ASTRO-MED ASC-951 PRESSURE PROCESSOR received FDA 510(k) clearance on 1990-01-18, under 510(k) number K894295.

Who is the listed applicant for ASTRO-MED ASC-951 PRESSURE PROCESSOR?

The FDA 510(k) record lists Astro-Med, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ASTRO-MED ASC-951 PRESSURE PROCESSOR?

The FDA product code for ASTRO-MED ASC-951 PRESSURE PROCESSOR is DRQ.

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Related Devices (Code: DRQ)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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