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FDA 510(k)

CAUTERY CLAMP AND BATTERY PACK POWER SUPPLY

K-Number: K992460 · 1999-10-05

ApplicantStarion Instruments
Decision Date1999-10-05
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CAUTERY CLAMP AND BATTERY PACK POWER SUPPLY is the device name listed in this FDA 510(k) record. The listed applicant is Starion Instruments. It received FDA 510(k) clearance on 1999-10-05 under 510(k) number K992460. 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 CAUTERY CLAMP AND BATTERY PACK POWER SUPPLY?

CAUTERY CLAMP AND BATTERY PACK POWER SUPPLY is a medical device that received FDA 510(k) clearance on 1999-10-05. The listed applicant is Starion Instruments. The 510(k) number is K992460.

When did CAUTERY CLAMP AND BATTERY PACK POWER SUPPLY receive FDA 510(k) clearance?

CAUTERY CLAMP AND BATTERY PACK POWER SUPPLY received FDA 510(k) clearance on 1999-10-05, under 510(k) number K992460.

Who is the listed applicant for CAUTERY CLAMP AND BATTERY PACK POWER SUPPLY?

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 CAUTERY CLAMP AND BATTERY PACK POWER SUPPLY?

The FDA product code for CAUTERY CLAMP AND BATTERY PACK POWER SUPPLY 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)

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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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