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FDA 510(k)

DISPOSABLE CAUTERY ABRASIVE PAD

K-Number: K915064 · 1992-03-11

ApplicantAmerican Medical Mfg., Inc.
Decision Date1992-03-11
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE CAUTERY ABRASIVE PAD is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Mfg., Inc.. It received FDA 510(k) clearance on 1992-03-11 under 510(k) number K915064. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE CAUTERY ABRASIVE PAD?

DISPOSABLE CAUTERY ABRASIVE PAD is a medical device that received FDA 510(k) clearance on 1992-03-11. The listed applicant is American Medical Mfg., Inc.. The 510(k) number is K915064.

When did DISPOSABLE CAUTERY ABRASIVE PAD receive FDA 510(k) clearance?

DISPOSABLE CAUTERY ABRASIVE PAD received FDA 510(k) clearance on 1992-03-11, under 510(k) number K915064.

Who is the listed applicant for DISPOSABLE CAUTERY ABRASIVE PAD?

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

What is the FDA product code for DISPOSABLE CAUTERY ABRASIVE PAD?

The FDA product code for DISPOSABLE CAUTERY ABRASIVE PAD is KDC.

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 American Medical Mfg., 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.

K982029SHARPS COLLECTION CONTAINER - SAF-T-SHELLK961454AMMI MAGNI-GUARDK915066DISPOSABLE SKIN MARKERK915065I.V.IRRIGATION POLEK915068PLASTIC DISPOSABLE SURGICAL LIGHT HANDLE COVER

Related Devices (Code: KDC)

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.

K943229DISPOSABLE SURGICAL SCISSORS AND FORCEPSY.M.K. International Co., Ltd.K936226SURGIMED BREAST LOCALIZATION NEEDLE WIRE SETMeadox Medicals, Div. Boston Scientific Corp.K920153THERMUFF BAGTechstylesK920263MANUAL SURGICAL INSTRUMENTSPhoenix Instruments Div.K914960INSTRUMENT ORGANIZERO.R. Concepts, Inc.K912834SHUR-GRIPInman Medical Corp.

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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