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FDA 510(k)

TISSUE SECTION ADHESIVE

K-Number: K881659 · 1988-04-21

ApplicantSurgipath Medical Industries, Inc.
Decision Date1988-04-21
Product CodeIFZ
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

TISSUE SECTION ADHESIVE is the device name listed in this FDA 510(k) record. The listed applicant is Surgipath Medical Industries, Inc.. It received FDA 510(k) clearance on 1988-04-21 under 510(k) number K881659. The device is classified under product code IFZ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TISSUE SECTION ADHESIVE?

TISSUE SECTION ADHESIVE is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Surgipath Medical Industries, Inc.. The 510(k) number is K881659.

When did TISSUE SECTION ADHESIVE receive FDA 510(k) clearance?

TISSUE SECTION ADHESIVE received FDA 510(k) clearance on 1988-04-21, under 510(k) number K881659.

Who is the listed applicant for TISSUE SECTION ADHESIVE?

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

What is the FDA product code for TISSUE SECTION ADHESIVE?

The FDA product code for TISSUE SECTION ADHESIVE is IFZ.

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Other records listing Surgipath Medical 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.

K883217SCHIFF REAGENTK881921C-E BRUSHK881922CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVEK863549REUSABLE/DISPOSABLE AUTOPSY KNIFE SETK863616KNIFE MAKERK863548ROTARY MICROTOME

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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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