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FDA 510(k)

ACROMED WALLIE-HEINIG TROCHAR

K-Number: K870779 · 1987-03-09

ApplicantBuckman Co., Inc.
Decision Date1987-03-09
Product CodeHWJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACROMED WALLIE-HEINIG TROCHAR 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 K870779. The device is classified under product code HWJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACROMED WALLIE-HEINIG TROCHAR?

ACROMED WALLIE-HEINIG TROCHAR 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 K870779.

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

ACROMED WALLIE-HEINIG TROCHAR received FDA 510(k) clearance on 1987-03-09, under 510(k) number K870779.

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

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 TROCHAR?

The FDA product code for ACROMED WALLIE-HEINIG TROCHAR is HWJ.

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Related Devices (Code: HWJ)

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.

K895587CROSS MEDICAL PRODUCT PEDICLE AWLCross Medical Products, Inc.K880045ACROMED AWL/PUNCH, DEPTH GAUGEBuckman Co., Inc.K875223DANNINGER ORTHOPAEDIC AWLDanninger Medical Technology, 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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