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FDA 510(k)

DISPOS. ACU-CUT SOFT TISSUE BIOPSY

K-Number: K842091 · 1984-07-23

ApplicantThe Healthcare Group Laboratories, Inc.
Decision Date1984-07-23
Product Code
DecisionSubstantially Equivalent

Device Summary

DISPOS. ACU-CUT SOFT TISSUE BIOPSY is the device name listed in this FDA 510(k) record. The listed applicant is The Healthcare Group Laboratories, Inc.. It received FDA 510(k) clearance on 1984-07-23 under 510(k) number K842091. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOS. ACU-CUT SOFT TISSUE BIOPSY?

DISPOS. ACU-CUT SOFT TISSUE BIOPSY is a medical device that received FDA 510(k) clearance on 1984-07-23. The listed applicant is The Healthcare Group Laboratories, Inc.. The 510(k) number is K842091.

When did DISPOS. ACU-CUT SOFT TISSUE BIOPSY receive FDA 510(k) clearance?

DISPOS. ACU-CUT SOFT TISSUE BIOPSY received FDA 510(k) clearance on 1984-07-23, under 510(k) number K842091.

Who is the listed applicant for DISPOS. ACU-CUT SOFT TISSUE BIOPSY?

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

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Other records listing The Healthcare Group Laboratories, 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.

K850035EMPTY SOLUTION TRANSFER CONTAINERK842170EMPTY SOLUTION TRANSFER CONTAINERK840742RIGHT ATRIAL CATHETERK830299SOLUTION TRANSFER CONTAINERK822307ADHESIVE SPRAY #4050-4060K822059SHOW'RBAG

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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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