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FDA 510(k)

TRACTION DEVICES, INTERMITTENT, TX

K-Number: K770724 · 1977-07-11

Decision Date1977-07-11
Product CodeIRS
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TRACTION DEVICES, INTERMITTENT, TX is the device name listed in this FDA 510(k) record. The listed applicant is Chattanooga Pharmacal Co.. It received FDA 510(k) clearance on 1977-07-11 under 510(k) number K770724. The device is classified under product code IRS. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRACTION DEVICES, INTERMITTENT, TX?

TRACTION DEVICES, INTERMITTENT, TX is a medical device that received FDA 510(k) clearance on 1977-07-11. The listed applicant is Chattanooga Pharmacal Co.. The 510(k) number is K770724.

When did TRACTION DEVICES, INTERMITTENT, TX receive FDA 510(k) clearance?

TRACTION DEVICES, INTERMITTENT, TX received FDA 510(k) clearance on 1977-07-11, under 510(k) number K770724.

Who is the listed applicant for TRACTION DEVICES, INTERMITTENT, TX?

The FDA 510(k) record lists Chattanooga Pharmacal Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRACTION DEVICES, INTERMITTENT, TX?

The FDA product code for TRACTION DEVICES, INTERMITTENT, TX is IRS.

Related Clinical Trials

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.

Other records listing Chattanooga Pharmacal Co. 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.

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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