STRYKER MPS ACUTE CARE BED
K-Number: K931482 · 1993-09-09
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Device Summary
Frequently Asked Questions
What is the STRYKER MPS ACUTE CARE BED?
STRYKER MPS ACUTE CARE BED is a medical device that received FDA 510(k) clearance on 1993-09-09. The listed applicant is Stryker Corp.. The 510(k) number is K931482.
When did STRYKER MPS ACUTE CARE BED receive FDA 510(k) clearance?
STRYKER MPS ACUTE CARE BED received FDA 510(k) clearance on 1993-09-09, under 510(k) number K931482.
Who is the listed applicant for STRYKER MPS ACUTE CARE BED?
The FDA 510(k) record lists Stryker Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STRYKER MPS ACUTE CARE BED?
The FDA product code for STRYKER MPS ACUTE 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 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.
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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