SURGISTAT
K-Number: K922206 · 1993-09-07
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Device Summary
Frequently Asked Questions
What is the SURGISTAT?
SURGISTAT is a medical device that received FDA 510(k) clearance on 1993-09-07. The listed applicant is Valleylab, Inc.. The 510(k) number is K922206.
When did SURGISTAT receive FDA 510(k) clearance?
SURGISTAT received FDA 510(k) clearance on 1993-09-07, under 510(k) number K922206.
Who is the listed applicant for SURGISTAT?
The FDA 510(k) record lists Valleylab, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SURGISTAT?
The FDA product code for SURGISTAT is HGI.
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 Valleylab, 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: HGI)
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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