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FDA 510(k)

STRYKER 5000

K-Number: K935949 · 1994-06-17

ApplicantStryker Medical
Decision Date1994-06-17
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRYKER 5000 is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Medical. It received FDA 510(k) clearance on 1994-06-17 under 510(k) number K935949. 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 STRYKER 5000?

STRYKER 5000 is a medical device that received FDA 510(k) clearance on 1994-06-17. The listed applicant is Stryker Medical. The 510(k) number is K935949.

When did STRYKER 5000 receive FDA 510(k) clearance?

STRYKER 5000 received FDA 510(k) clearance on 1994-06-17, under 510(k) number K935949.

Who is the listed applicant for STRYKER 5000?

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

What is the FDA product code for STRYKER 5000?

The FDA product code for STRYKER 5000 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 Stryker Medical 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.

K222818Xpedition ™ Powered Stair Chair (625700000000)K180834Altrix Precision Temperature Management SystemK171149Altrix Temperature Management WrapsK152266Altrix Precision Temperature Management SystemK113598POWER-LOAD COT FASTENER SYSTEMK946149STRYKER AGILITY INTENSIVE CARE BED

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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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