STRYKER AGILITY INTENSIVE CARE BED
K-Number: K946149 · 1995-03-14
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Device Summary
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.
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
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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