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FDA 510(k)

ACROMED WALLIE-HEINIG DISECTOR/ELEVATORS

K-Number: K870781 · 1987-03-09

ApplicantBuckman Co., Inc.
Decision Date1987-03-09
Product CodeGEG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ACROMED WALLIE-HEINIG DISECTOR/ELEVATORS is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1987-03-09 under 510(k) number K870781. The device is classified under product code GEG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACROMED WALLIE-HEINIG DISECTOR/ELEVATORS?

ACROMED WALLIE-HEINIG DISECTOR/ELEVATORS is a medical device that received FDA 510(k) clearance on 1987-03-09. The listed applicant is Buckman Co., Inc.. The 510(k) number is K870781.

When did ACROMED WALLIE-HEINIG DISECTOR/ELEVATORS receive FDA 510(k) clearance?

ACROMED WALLIE-HEINIG DISECTOR/ELEVATORS received FDA 510(k) clearance on 1987-03-09, under 510(k) number K870781.

Who is the listed applicant for ACROMED WALLIE-HEINIG DISECTOR/ELEVATORS?

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

What is the FDA product code for ACROMED WALLIE-HEINIG DISECTOR/ELEVATORS?

The FDA product code for ACROMED WALLIE-HEINIG DISECTOR/ELEVATORS is GEG.

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Related Devices (Code: GEG)

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.

K891894ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSEZinnanti Surgical Instruments, Inc.K891899ELEVATORS, VARIOUS TYPESZinnanti Surgical Instruments, Inc.K890365SEPTUM ELEVATORKinetic Medical ProductsK890253SURGICAL ELEVATORKinetic Medical ProductsK890230LIGATURE NEEDLESKinetic Medical ProductsK8724911.1 TWIST DRILLS AND 1.2 CORTICAL DRILLSMicro-Aire Surgical Instruments, 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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