FDA 510(k)

TPG 1000

K-Number: K831002 · 1983-06-24

Decision Date1983-06-24

Product CodeKQZ

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

TPG 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Physical Diagnostics, Inc.. It received FDA 510(k) clearance on 1983-06-24 under 510(k) number K831002. The device is classified under product code KQZ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TPG 1000?

TPG 1000 is a medical device that received FDA 510(k) clearance on 1983-06-24. The listed applicant is Physical Diagnostics, Inc.. The 510(k) number is K831002.

When did TPG 1000 receive FDA 510(k) clearance?

TPG 1000 received FDA 510(k) clearance on 1983-06-24, under 510(k) number K831002.

Who is the listed applicant for TPG 1000?

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

What is the FDA product code for TPG 1000?

The FDA product code for TPG 1000 is KQZ.

Related Devices (Code: KQZ)

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.

K884132TECNOL BUCKS TRACTION W/HEEL PROTECTORTechnol, Inc.K882640TECNOL SECURE-ALL PELVIC TRACTION BELTTecnol New Jersey Wound Care, Inc.K871900OVER DRAPE LEG HOLDERAvec Scientific Design Corp.K871296T.E.D.(TM) TRACTION DEVICEThe Kendal Co.K854270MURPHY ADJUSTABLE SPLINTComfortex, Inc.K823660UNIVERSAL BUCKS TRACTIONWarm & Form, Orthopedic Materials

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.