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FDA 510(k)

SURGICAL DESIGN CORPORATION MODEL 700 LOW PRESSURE MATTRESS

K-Number: K934817 · 1994-06-17

ApplicantSurgical Design Corp.
Decision Date1994-06-17
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SURGICAL DESIGN CORPORATION MODEL 700 LOW PRESSURE MATTRESS is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Design Corp.. It received FDA 510(k) clearance on 1994-06-17 under 510(k) number K934817. 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 SURGICAL DESIGN CORPORATION MODEL 700 LOW PRESSURE MATTRESS?

SURGICAL DESIGN CORPORATION MODEL 700 LOW PRESSURE MATTRESS is a medical device that received FDA 510(k) clearance on 1994-06-17. The listed applicant is Surgical Design Corp.. The 510(k) number is K934817.

When did SURGICAL DESIGN CORPORATION MODEL 700 LOW PRESSURE MATTRESS receive FDA 510(k) clearance?

SURGICAL DESIGN CORPORATION MODEL 700 LOW PRESSURE MATTRESS received FDA 510(k) clearance on 1994-06-17, under 510(k) number K934817.

Who is the listed applicant for SURGICAL DESIGN CORPORATION MODEL 700 LOW PRESSURE MATTRESS?

The FDA 510(k) record lists Surgical Design Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICAL DESIGN CORPORATION MODEL 700 LOW PRESSURE MATTRESS?

The FDA product code for SURGICAL DESIGN CORPORATION MODEL 700 LOW PRESSURE MATTRESS is FNM.

Related Clinical Trials

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.

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Other records listing Surgical Design Corp. as applicant

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.

K991852OCUSYSTEM ART ADVANTAGE, MODEL 995K961243OCUSYSTEM ART ADVANTAGE

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

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

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