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FDA 510(k)

GUS TRAC C-303

K-Number: K872780 · 1987-10-06

ApplicantGus Company, Inc.
Decision Date1987-10-06
Product CodeITH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GUS TRAC C-303 is the device name listed in this FDA 510(k) record. The listed applicant is Gus Company, Inc.. It received FDA 510(k) clearance on 1987-10-06 under 510(k) number K872780. The device is classified under product code ITH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GUS TRAC C-303?

GUS TRAC C-303 is a medical device that received FDA 510(k) clearance on 1987-10-06. The listed applicant is Gus Company, Inc.. The 510(k) number is K872780.

When did GUS TRAC C-303 receive FDA 510(k) clearance?

GUS TRAC C-303 received FDA 510(k) clearance on 1987-10-06, under 510(k) number K872780.

Who is the listed applicant for GUS TRAC C-303?

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

What is the FDA product code for GUS TRAC C-303?

The FDA product code for GUS TRAC C-303 is ITH.

Related Devices (Code: ITH)

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.

K243775True Non-Surgical Spinal Decompression System (DRX9000-SL)Excite Medical of Tampa Bay, LLCK243366DRX9000C-SL Cervical Spinal Decompression SystemExcite Medical of Tampa Bay, LLCK214037Ergo-Flex Technologies Back on Trac (BOTGEN1) and Cervi-TracErgo-Flex Technologies, LLCK222912c1TracZimmer Medizinsysteme GmbHK112074EVERYWAY TRACTION UNIT, MODEL EVER-TRAC ET-800Everyway Medical Instruments Co.,LtdK103248INTEGRITY SPINAL CARE SYSTEMIntegra Life Sciences

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.

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