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FDA 510(k)

PERI-PATCH PERITONEAL CATHETER EXTENSION

K-Number: K810531 · 1981-03-24

ApplicantQuinton, Inc.
Decision Date1981-03-24
Product CodeKGZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PERI-PATCH PERITONEAL CATHETER EXTENSION is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1981-03-24 under 510(k) number K810531. The device is classified under product code KGZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERI-PATCH PERITONEAL CATHETER EXTENSION?

PERI-PATCH PERITONEAL CATHETER EXTENSION is a medical device that received FDA 510(k) clearance on 1981-03-24. The listed applicant is Quinton, Inc.. The 510(k) number is K810531.

When did PERI-PATCH PERITONEAL CATHETER EXTENSION receive FDA 510(k) clearance?

PERI-PATCH PERITONEAL CATHETER EXTENSION received FDA 510(k) clearance on 1981-03-24, under 510(k) number K810531.

Who is the listed applicant for PERI-PATCH PERITONEAL CATHETER EXTENSION?

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

What is the FDA product code for PERI-PATCH PERITONEAL CATHETER EXTENSION?

The FDA product code for PERI-PATCH PERITONEAL CATHETER EXTENSION is KGZ.

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Other records listing Quinton, Inc. as applicant

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Related Devices (Code: KGZ)

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.

K022306AART SILICONE TUBINGAesthetic and Reconstructive Technologies, Inc.K974295BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBINGByron MedicalK973183WOUND DRAINAGE HOLDERR & D Medical Products, Inc.K955433DURALASTIC SILICONE TUBINGAllied Biomedical Corp.K942315NAVARRE PERCUTANEOUS ACCESS SETNavarre Biomedical , Ltd.K896087PALESTRANT IRRIGATION AND DRAINAGE SETNorth American Instrument Corp.

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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