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FDA 510(k)

EQUI-PISE 1000 MRS

K-Number: K970350 · 1997-04-22

ApplicantAdvanced Air Support Consultancy, Inc.
Decision Date1997-04-22
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EQUI-PISE 1000 MRS is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Air Support Consultancy, Inc.. It received FDA 510(k) clearance on 1997-04-22 under 510(k) number K970350. The device is classified under product code FNM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EQUI-PISE 1000 MRS?

EQUI-PISE 1000 MRS is a medical device that received FDA 510(k) clearance on 1997-04-22. The listed applicant is Advanced Air Support Consultancy, Inc.. The 510(k) number is K970350.

When did EQUI-PISE 1000 MRS receive FDA 510(k) clearance?

EQUI-PISE 1000 MRS received FDA 510(k) clearance on 1997-04-22, under 510(k) number K970350.

Who is the listed applicant for EQUI-PISE 1000 MRS?

The FDA 510(k) record lists Advanced Air Support Consultancy, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EQUI-PISE 1000 MRS?

The FDA product code for EQUI-PISE 1000 MRS is FNM.

Related Devices (Code: FNM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K973169PRESSURE GUARD SITE SELECT (A)Span-America Medical Systems, Inc.K972022ZAK-2000Cardio Systems, Inc.K974319MIGHTY AIRWheelchairs of KansasK974070PHYSIO/1000Physio Designs, Inc.K972549SIMPULSEKinetic Concepts, Inc.K970081SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEMCathay Consolidated, Inc.

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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