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FDA 510(k)

TISSUE PUNCH

K-Number: K882834 · 1988-08-02

Decision Date1988-08-02
Product CodeEKJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TISSUE PUNCH is the device name listed in this FDA 510(k) record. The listed applicant is Tri-Stage, Inc.. It received FDA 510(k) clearance on 1988-08-02 under 510(k) number K882834. The device is classified under product code EKJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TISSUE PUNCH?

TISSUE PUNCH is a medical device that received FDA 510(k) clearance on 1988-08-02. The listed applicant is Tri-Stage, Inc.. The 510(k) number is K882834.

When did TISSUE PUNCH receive FDA 510(k) clearance?

TISSUE PUNCH received FDA 510(k) clearance on 1988-08-02, under 510(k) number K882834.

Who is the listed applicant for TISSUE PUNCH?

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

What is the FDA product code for TISSUE PUNCH?

The FDA product code for TISSUE PUNCH is EKJ.

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 Tri-Stage, 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.

Related Devices (Code: EKJ)

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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