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FDA 510(k)

REPLACABLE BATTERY HI-TEMP CAUTERY

K-Number: K810014 · 1981-02-12

ApplicantMedical Products Development, Inc.
Decision Date1981-02-12
Product CodeHAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REPLACABLE BATTERY HI-TEMP 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 1981-02-12 under 510(k) number K810014. The device is classified under product code HAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPLACABLE BATTERY HI-TEMP CAUTERY?

REPLACABLE BATTERY HI-TEMP CAUTERY is a medical device that received FDA 510(k) clearance on 1981-02-12. The listed applicant is Medical Products Development, Inc.. The 510(k) number is K810014.

When did REPLACABLE BATTERY HI-TEMP CAUTERY receive FDA 510(k) clearance?

REPLACABLE BATTERY HI-TEMP CAUTERY received FDA 510(k) clearance on 1981-02-12, under 510(k) number K810014.

Who is the listed applicant for REPLACABLE BATTERY HI-TEMP 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 REPLACABLE BATTERY HI-TEMP CAUTERY?

The FDA product code for REPLACABLE BATTERY HI-TEMP CAUTERY is HAM.

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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.

K810013MULTIPERFECTEMP CAUTERYK810016REPLACABLE BATTERY PERFECTEMP CAUTERYK810012MULTIMICRO SURGICAL CAUTERYK803067SURG-FLEX 10 LIGHTK810015MULTIHI-TEMP CAUTERYK802942HITEMP. TM 2 LOOPTIP CAUTERY

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Related Devices (Code: HAM)

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.

K153472Quiver Laparoscopic ExtendableItl Corporation Pty, Ltd.K000079NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777MNikomed U.S.A., Inc.K993306NIKOPAD ELECTROSURGICAL GROUNDING PAD (*OR SOLD UNDER COMMERCIAL NAMES), MODEL 4760 (TYPICALLY)Paladin Medical, Inc.K945861BERGEN 710 ESUBergen Mfg.K913300LAPAROSTAT(TM)Cook Ob/GynK920100GSU HANDPIECE ADAPTERBeacon Laboratories, 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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