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FDA 510(k)

MICRO CAUTERY

K-Number: K810909 · 1981-04-17

ApplicantKey Medical, Inc.
Decision Date1981-04-17
Product CodeHAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICRO CAUTERY is the device name listed in this FDA 510(k) record. The listed applicant is Key Medical, Inc.. It received FDA 510(k) clearance on 1981-04-17 under 510(k) number K810909. 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 MICRO CAUTERY?

MICRO CAUTERY is a medical device that received FDA 510(k) clearance on 1981-04-17. The listed applicant is Key Medical, Inc.. The 510(k) number is K810909.

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

MICRO CAUTERY received FDA 510(k) clearance on 1981-04-17, under 510(k) number K810909.

Who is the listed applicant for MICRO CAUTERY?

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

What is the FDA product code for MICRO CAUTERY?

The FDA product code for MICRO CAUTERY is HAM.

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.

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Other records listing Key Medical, 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.

K821127KEY DRILLK812760HI-TEMP CARDIOVASCULAR CAUTERYK812644REPLACEABLE BATTERY PERFECTEMP 2 CAUT

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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