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FDA 510(k)

PELVIC TRACTION BELT

K-Number: K823659 · 1982-12-30

Decision Date1982-12-30
Product CodeILZ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PELVIC TRACTION BELT is the device name listed in this FDA 510(k) record. The listed applicant is Warm & Form, Orthopedic Materials. It received FDA 510(k) clearance on 1982-12-30 under 510(k) number K823659. The device is classified under product code ILZ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PELVIC TRACTION BELT?

PELVIC TRACTION BELT is a medical device that received FDA 510(k) clearance on 1982-12-30. The listed applicant is Warm & Form, Orthopedic Materials. The 510(k) number is K823659.

When did PELVIC TRACTION BELT receive FDA 510(k) clearance?

PELVIC TRACTION BELT received FDA 510(k) clearance on 1982-12-30, under 510(k) number K823659.

Who is the listed applicant for PELVIC TRACTION BELT?

The FDA 510(k) record lists Warm & Form, Orthopedic Materials as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PELVIC TRACTION BELT?

The FDA product code for PELVIC TRACTION BELT is ILZ.

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 Warm & Form, Orthopedic Materials 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.

View all 24 devices →

Related Devices (Code: ILZ)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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