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FDA 510(k)

THERMAL CAUTERY UNIT, MODEL 150

K-Number: K002341 · 2000-10-23

ApplicantGeiger Medical Technologies, Inc.
Decision Date2000-10-23
Product CodeHQO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

THERMAL CAUTERY UNIT, MODEL 150 is the device name listed in this FDA 510(k) record. The listed applicant is Geiger Medical Technologies, Inc.. It received FDA 510(k) clearance on 2000-10-23 under 510(k) number K002341. The device is classified under product code HQO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERMAL CAUTERY UNIT, MODEL 150?

THERMAL CAUTERY UNIT, MODEL 150 is a medical device that received FDA 510(k) clearance on 2000-10-23. The listed applicant is Geiger Medical Technologies, Inc.. The 510(k) number is K002341.

When did THERMAL CAUTERY UNIT, MODEL 150 receive FDA 510(k) clearance?

THERMAL CAUTERY UNIT, MODEL 150 received FDA 510(k) clearance on 2000-10-23, under 510(k) number K002341.

Who is the listed applicant for THERMAL CAUTERY UNIT, MODEL 150?

The FDA 510(k) record lists Geiger Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THERMAL CAUTERY UNIT, MODEL 150?

The FDA product code for THERMAL CAUTERY UNIT, MODEL 150 is HQO.

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Other records listing Geiger Medical Technologies, Inc. as applicant

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Related Devices (Code: HQO)

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 SUPPLYStarion InstrumentsK043155STARION UNIVERSAL POWER SUPPLY (UPS)Starion InstrumentsK000893AC POWERED THERMAL CAUTERY UNITStarion InstrumentsK971538MENTOR GEMINI HEMOSTATIC ERASERMentor Ophthalmics, Inc.K962135D.O.R.C. MICRODIATHERMY SYSTEMDutch Ophthalmic USA, Inc.K943031BIPOLAR ELECTROSURGICAL PENCILBoston Surgical Products, Inc.

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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