FDA 510(k)

PROT-A-TRAC

K-Number: K802072 · 1980-09-26

Decision Date1980-09-26

Product CodeHST

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

PROT-A-TRAC is the device name listed in this FDA 510(k) record. The listed applicant is Robert I. Branick, M.D.. It received FDA 510(k) clearance on 1980-09-26 under 510(k) number K802072. The device is classified under product code HST. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROT-A-TRAC?

PROT-A-TRAC is a medical device that received FDA 510(k) clearance on 1980-09-26. The listed applicant is Robert I. Branick, M.D.. The 510(k) number is K802072.

When did PROT-A-TRAC receive FDA 510(k) clearance?

PROT-A-TRAC received FDA 510(k) clearance on 1980-09-26, under 510(k) number K802072.

Who is the listed applicant for PROT-A-TRAC?

The FDA 510(k) record lists Robert I. Branick, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROT-A-TRAC?

The FDA product code for PROT-A-TRAC is HST.

Related Devices (Code: HST)

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.

K162702Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression TableStl International, Inc.K110858LO-BAK TRAXRoland F Berthiaume, DC K984190BACK-ON-TRAC, MODEL 101BOTBack-On-Track, Inc.K872121K AND D HOME TRACTJoseph A. Kott, M.D.K870212ARTHROSCOPIC SHOULDER HOLDERDyonics, Inc.K870125EXTREMITY ELEVATOROrthopedic Systems, Inc.

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.