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FDA 510(k)

AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTS

K-Number: K924725 · 1993-02-05

ApplicantAmerican Biomaterials Corp.
Decision Date1993-02-05
Product CodeMDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is American Biomaterials Corp.. It received FDA 510(k) clearance on 1993-02-05 under 510(k) number K924725. The device is classified under product code MDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTS?

AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1993-02-05. The listed applicant is American Biomaterials Corp.. The 510(k) number is K924725.

When did AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTS receive FDA 510(k) clearance?

AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTS received FDA 510(k) clearance on 1993-02-05, under 510(k) number K924725.

Who is the listed applicant for AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTS?

The FDA 510(k) record lists American Biomaterials Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTS?

The FDA product code for AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTS is MDM.

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 Biomaterials Corp. 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.

K922455EVERT-O-CATH CATHETERK915824HOLE PUNCHK880371BIOGLASS DENTAL ENDOSSEOUS RIDGE MAINTAINERK863796CREATIVE CARE SYSTEMS' IV START KITK843461BIOGLASS OSSICULAR RECONSTRUCTION PROSTH

Related Devices (Code: MDM)

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.

K073664FRONTLINE MEDICAL SAFETYNET GUIDEWIRE INTRODUCERInjectimed, Inc.K050575FUTUMEDS NO PATIENT CONTACT SAFETY LANCET WITH PALS SYSTEMFutumeds Sdn BhdK050957EUTROCHARSpecial Devices, Inc.K023173ANDREWS INTRODUCER, MODEL ASI01Andrews Surgical Innovations, Ltd.K022059MICROVASIVE PULMONARY GUIDEWIREBoston Scientific CorpK013040LIGHT SABER INTRODUCER NEEDLEMinrad, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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