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FDA 510(k)

STRYKER AGILITY INTENSIVE CARE BED

K-Number: K946149 · 1995-03-14

Decision Date1995-03-14
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRYKER AGILITY INTENSIVE CARE BED is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Medical. It received FDA 510(k) clearance on 1995-03-14 under 510(k) number K946149. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER AGILITY INTENSIVE CARE BED?

STRYKER AGILITY INTENSIVE CARE BED is a medical device that received FDA 510(k) clearance on 1995-03-14. The listed applicant is Stryker Medical. The 510(k) number is K946149.

When did STRYKER AGILITY INTENSIVE CARE BED receive FDA 510(k) clearance?

STRYKER AGILITY INTENSIVE CARE BED received FDA 510(k) clearance on 1995-03-14, under 510(k) number K946149.

Who is the listed applicant for STRYKER AGILITY INTENSIVE CARE BED?

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 AGILITY INTENSIVE CARE BED?

The FDA product code for STRYKER AGILITY INTENSIVE CARE BED is FNL.

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.

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.

View all 14 devices →

Related Devices (Code: FNL)

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.

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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