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FDA 510(k)

VARIOUS STERILE BIOPSY ASPIRATION NEED

K-Number: K821017 · 1982-06-22

Decision Date1982-06-22
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VARIOUS STERILE BIOPSY ASPIRATION NEED is the device name listed in this FDA 510(k) record. The listed applicant is Medsurg Industries, Inc.. It received FDA 510(k) clearance on 1982-06-22 under 510(k) number K821017. The device is classified under product code GAA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARIOUS STERILE BIOPSY ASPIRATION NEED?

VARIOUS STERILE BIOPSY ASPIRATION NEED is a medical device that received FDA 510(k) clearance on 1982-06-22. The listed applicant is Medsurg Industries, Inc.. The 510(k) number is K821017.

When did VARIOUS STERILE BIOPSY ASPIRATION NEED receive FDA 510(k) clearance?

VARIOUS STERILE BIOPSY ASPIRATION NEED received FDA 510(k) clearance on 1982-06-22, under 510(k) number K821017.

Who is the listed applicant for VARIOUS STERILE BIOPSY ASPIRATION NEED?

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

What is the FDA product code for VARIOUS STERILE BIOPSY ASPIRATION NEED?

The FDA product code for VARIOUS STERILE BIOPSY ASPIRATION NEED is GAA.

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.

Other records listing Medsurg Industries, 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.

View all 41 devices →

Related Devices (Code: GAA)

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.

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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