BK-6157-02 C.V.A SLING, MEDIUM&LARGE
K-Number: K801713 · 1980-08-07
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Device Summary
Frequently Asked Questions
What is the BK-6157-02 C.V.A SLING, MEDIUM&LARGE?
BK-6157-02 C.V.A SLING, MEDIUM&LARGE is a medical device that received FDA 510(k) clearance on 1980-08-07. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K801713.
When did BK-6157-02 C.V.A SLING, MEDIUM&LARGE receive FDA 510(k) clearance?
BK-6157-02 C.V.A SLING, MEDIUM&LARGE received FDA 510(k) clearance on 1980-08-07, under 510(k) number K801713.
Who is the listed applicant for BK-6157-02 C.V.A SLING, MEDIUM&LARGE?
The FDA 510(k) record lists Fred Sammons, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BK-6157-02 C.V.A SLING, MEDIUM&LARGE?
The FDA product code for BK-6157-02 C.V.A SLING, MEDIUM&LARGE is ILI.
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 Fred Sammons, 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: ILI)
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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