CART, ORTHOPEDIC BED, STRYKER
K-Number: K863685 · 1987-01-15
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Device Summary
Frequently Asked Questions
What is the CART, ORTHOPEDIC BED, STRYKER?
CART, ORTHOPEDIC BED, STRYKER is a medical device that received FDA 510(k) clearance on 1987-01-15. The listed applicant is Brenner Metal Prod Corp.. The 510(k) number is K863685.
When did CART, ORTHOPEDIC BED, STRYKER receive FDA 510(k) clearance?
CART, ORTHOPEDIC BED, STRYKER received FDA 510(k) clearance on 1987-01-15, under 510(k) number K863685.
Who is the listed applicant for CART, ORTHOPEDIC BED, STRYKER?
The FDA 510(k) record lists Brenner Metal Prod Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CART, ORTHOPEDIC BED, STRYKER?
The FDA product code for CART, ORTHOPEDIC BED, STRYKER is FNJ.
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 Brenner Metal Prod 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: FNJ)
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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