VAIL 2000 ENCLOSED BED
K-Number: K963622 · 1997-05-07
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Device Summary
Frequently Asked Questions
What is the VAIL 2000 ENCLOSED BED?
VAIL 2000 ENCLOSED BED is a medical device that received FDA 510(k) clearance on 1997-05-07. The listed applicant is Vail Products, Inc.. The 510(k) number is K963622.
When did VAIL 2000 ENCLOSED BED receive FDA 510(k) clearance?
VAIL 2000 ENCLOSED BED received FDA 510(k) clearance on 1997-05-07, under 510(k) number K963622.
Who is the listed applicant for VAIL 2000 ENCLOSED BED?
The FDA 510(k) record lists Vail Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VAIL 2000 ENCLOSED BED?
The FDA product code for VAIL 2000 ENCLOSED 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 Vail Products, 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: 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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