THERMAL CAUTERY DEVICE, FORCEPS
K-Number: K990728 · 1999-06-03
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Device Summary
Frequently Asked Questions
What is the THERMAL CAUTERY DEVICE, FORCEPS?
THERMAL CAUTERY DEVICE, FORCEPS is a medical device that received FDA 510(k) clearance on 1999-06-03. The listed applicant is Starion Instruments. The 510(k) number is K990728.
When did THERMAL CAUTERY DEVICE, FORCEPS receive FDA 510(k) clearance?
THERMAL CAUTERY DEVICE, FORCEPS received FDA 510(k) clearance on 1999-06-03, under 510(k) number K990728.
Who is the listed applicant for THERMAL CAUTERY DEVICE, FORCEPS?
The FDA 510(k) record lists Starion Instruments as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THERMAL CAUTERY DEVICE, FORCEPS?
The FDA product code for THERMAL CAUTERY DEVICE, FORCEPS is HQP.
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 Starion Instruments 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: HQP)
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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