FDA 510(k)

TM-CAPD

K-Number: K812615 · 1982-01-05

Decision Date1982-01-05

Product CodeKPP

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

TM-CAPD is the device name listed in this FDA 510(k) record. The listed applicant is Tri-Med, Inc.. It received FDA 510(k) clearance on 1982-01-05 under 510(k) number K812615. The device is classified under product code KPP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TM-CAPD?

TM-CAPD is a medical device that received FDA 510(k) clearance on 1982-01-05. The listed applicant is Tri-Med, Inc.. The 510(k) number is K812615.

When did TM-CAPD receive FDA 510(k) clearance?

TM-CAPD received FDA 510(k) clearance on 1982-01-05, under 510(k) number K812615.

Who is the listed applicant for TM-CAPD?

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

What is the FDA product code for TM-CAPD?

The FDA product code for TM-CAPD is KPP.

Other records listing Tri-Med, 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.

K040112TRIMED BEARING PLATE; TRIMED VOLAR BEARING PLATE K030877TRIMED RADIAL BULLET K010545TBW K961863PARACENTESIS TRAYS K875224HUDSON CRANINAL BURRS K850746TRI-MED MODEL 126 SAMPLE LINE W/EXTENDED LIFE NAFI

View all 29 devices →

Related Devices (Code: KPP)

K803275KPP PERITONEAL DIALYSATE FILTERMillipore Corp.K800666QUIK-TEMPLiquid Crystal Products, Inc.

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.