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FDA 510(k)

TAYLOR TRACTION CORD

K-Number: K792248 · 1979-11-30

ApplicantTaylor Medical Equipment
Decision Date1979-11-30
Product CodeHST
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TAYLOR TRACTION CORD is the device name listed in this FDA 510(k) record. The listed applicant is Taylor Medical Equipment. It received FDA 510(k) clearance on 1979-11-30 under 510(k) number K792248. 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 TAYLOR TRACTION CORD?

TAYLOR TRACTION CORD is a medical device that received FDA 510(k) clearance on 1979-11-30. The listed applicant is Taylor Medical Equipment. The 510(k) number is K792248.

When did TAYLOR TRACTION CORD receive FDA 510(k) clearance?

TAYLOR TRACTION CORD received FDA 510(k) clearance on 1979-11-30, under 510(k) number K792248.

Who is the listed applicant for TAYLOR TRACTION CORD?

The FDA 510(k) record lists Taylor Medical Equipment as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TAYLOR TRACTION CORD?

The FDA product code for TAYLOR TRACTION CORD is HST.

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.

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Other records listing Taylor Medical Equipment 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.

K792247TAYLOR PATIENT TRANSFER BOARD

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, DCK984190BACK-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

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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