SURGIPROBES AND SURGISCALPES IN HEAD/NECK SURGERY
K-Number: K894471 · 1989-11-14
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Device Summary
Frequently Asked Questions
What is the SURGIPROBES AND SURGISCALPES IN HEAD/NECK SURGERY?
SURGIPROBES AND SURGISCALPES IN HEAD/NECK SURGERY is a medical device that received FDA 510(k) clearance on 1989-11-14. The listed applicant is Surgilase, Inc.. The 510(k) number is K894471.
When did SURGIPROBES AND SURGISCALPES IN HEAD/NECK SURGERY receive FDA 510(k) clearance?
SURGIPROBES AND SURGISCALPES IN HEAD/NECK SURGERY received FDA 510(k) clearance on 1989-11-14, under 510(k) number K894471.
Who is the listed applicant for SURGIPROBES AND SURGISCALPES IN HEAD/NECK SURGERY?
The FDA 510(k) record lists Surgilase, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SURGIPROBES AND SURGISCALPES IN HEAD/NECK SURGERY?
The FDA product code for SURGIPROBES AND SURGISCALPES IN HEAD/NECK SURGERY is GEX. This falls under the Gastroenterology category.
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 Surgilase, 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: GEX)
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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