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FDA 510(k)

THERMAL CAUTERY FORCEPS

K-Number: K001262 · 2000-06-14

ApplicantStarion Instruments
Decision Date2000-06-14
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THERMAL CAUTERY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Starion Instruments. It received FDA 510(k) clearance on 2000-06-14 under 510(k) number K001262. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERMAL CAUTERY FORCEPS?

THERMAL CAUTERY FORCEPS is a medical device that received FDA 510(k) clearance on 2000-06-14. The listed applicant is Starion Instruments. The 510(k) number is K001262.

When did THERMAL CAUTERY FORCEPS receive FDA 510(k) clearance?

THERMAL CAUTERY FORCEPS received FDA 510(k) clearance on 2000-06-14, under 510(k) number K001262.

Who is the listed applicant for THERMAL CAUTERY 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 FORCEPS?

The FDA product code for THERMAL CAUTERY FORCEPS is GEI.

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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.

K070871STARION UNIVERSAL POWER SUPPLYK062257STARION INSTRUMENTS THERMAL LITIGATING SHEARSK050308THERMAL CAUTERY PROBEK043155STARION UNIVERSAL POWER SUPPLY (UPS)K002547STARION INSTRUMENTS POWER POINT CAUTERY GRASPER/DISSECTORK000893AC POWERED THERMAL CAUTERY UNIT

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Related Devices (Code: GEI)

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.

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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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