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FDA 510(k)

MULTIPERFECTEMP CAUTERY

K-Number: K810013 · 1981-04-23

ApplicantMedical Products Development, Inc.
Decision Date1981-04-23
Product CodeHQP
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MULTIPERFECTEMP CAUTERY is the device name listed in this FDA 510(k) record. The listed applicant is Medical Products Development, Inc.. It received FDA 510(k) clearance on 1981-04-23 under 510(k) number K810013. The device is classified under product code HQP. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPERFECTEMP CAUTERY?

MULTIPERFECTEMP CAUTERY is a medical device that received FDA 510(k) clearance on 1981-04-23. The listed applicant is Medical Products Development, Inc.. The 510(k) number is K810013.

When did MULTIPERFECTEMP CAUTERY receive FDA 510(k) clearance?

MULTIPERFECTEMP CAUTERY received FDA 510(k) clearance on 1981-04-23, under 510(k) number K810013.

Who is the listed applicant for MULTIPERFECTEMP CAUTERY?

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

What is the FDA product code for MULTIPERFECTEMP CAUTERY?

The FDA product code for MULTIPERFECTEMP CAUTERY 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Medical Products Development, 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.

K810012MULTIMICRO SURGICAL CAUTERYK810016REPLACABLE BATTERY PERFECTEMP CAUTERYK803067SURG-FLEX 10 LIGHTK810014REPLACABLE BATTERY HI-TEMP CAUTERYK810015MULTIHI-TEMP CAUTERYK802942HITEMP. TM 2 LOOPTIP CAUTERY

View all 13 devices →

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.

K121441CAUTERY; LOW TEMPERATURE (FINEADJUSTABLE FINE TIP, ELONGATED FINE TIP, MICRO FINE TIP)Bovie Medical CorporationK083428F7244, F7255, F7266, F7277, F7288, F7233, F7234 SERIES OF BATTERY-POWERED CAUTERYFiab SpaK062659KIRWAN DISPOSABLE BATTERY-POWERED CAUTERY, MODEL 41-61XX SERIESKirwan Surgical Products, Inc.K023506SURGICAL MEDICAL DEVICE CAUTERYModern Medical Equipment Mfg., Ltd.K002547STARION INSTRUMENTS POWER POINT CAUTERY GRASPER/DISSECTORStarion InstrumentsK994019CAUTERY GRASPER/DISSECTORStarion Instruments

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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