MODEL 35-B ALL LEVEL COT
K-Number: K864269 · 1986-11-13
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Device Summary
Frequently Asked Questions
What is the MODEL 35-B ALL LEVEL COT?
MODEL 35-B ALL LEVEL COT is a medical device that received FDA 510(k) clearance on 1986-11-13. The listed applicant is Ferno-Washington, Inc.. The 510(k) number is K864269.
When did MODEL 35-B ALL LEVEL COT receive FDA 510(k) clearance?
MODEL 35-B ALL LEVEL COT received FDA 510(k) clearance on 1986-11-13, under 510(k) number K864269.
Who is the listed applicant for MODEL 35-B ALL LEVEL COT?
The FDA 510(k) record lists Ferno-Washington, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL 35-B ALL LEVEL COT?
The FDA product code for MODEL 35-B ALL LEVEL COT is FPO.
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 Ferno-Washington, Inc. 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: FPO)
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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