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FDA 510(k)

ACROMED WALLIE-HEINIG CURETTES

K-Number: K870778 · 1987-03-09

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

Device Summary

ACROMED WALLIE-HEINIG CURETTES 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 K870778. The device is classified under product code HTF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACROMED WALLIE-HEINIG CURETTES?

ACROMED WALLIE-HEINIG CURETTES 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 K870778.

When did ACROMED WALLIE-HEINIG CURETTES receive FDA 510(k) clearance?

ACROMED WALLIE-HEINIG CURETTES received FDA 510(k) clearance on 1987-03-09, under 510(k) number K870778.

Who is the listed applicant for ACROMED WALLIE-HEINIG CURETTES?

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 CURETTES?

The FDA product code for ACROMED WALLIE-HEINIG CURETTES is HTF.

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Related Devices (Code: HTF)

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K890252BONE CURETTEKinetic Medical ProductsK8419794MM CUP CURRETTEStainless Mfg., 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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