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FDA 510(k)

BOGER AUTO-TRACTION DEVICE

K-Number: K820663 · 1982-05-03

ApplicantD.C. Medical Device, Inc.
Decision Date1982-05-03
Product CodeILZ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BOGER AUTO-TRACTION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is D.C. Medical Device, Inc.. It received FDA 510(k) clearance on 1982-05-03 under 510(k) number K820663. 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 BOGER AUTO-TRACTION DEVICE?

BOGER AUTO-TRACTION DEVICE is a medical device that received FDA 510(k) clearance on 1982-05-03. The listed applicant is D.C. Medical Device, Inc.. The 510(k) number is K820663.

When did BOGER AUTO-TRACTION DEVICE receive FDA 510(k) clearance?

BOGER AUTO-TRACTION DEVICE received FDA 510(k) clearance on 1982-05-03, under 510(k) number K820663.

Who is the listed applicant for BOGER AUTO-TRACTION DEVICE?

The FDA 510(k) record lists D.C. Medical Device, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BOGER AUTO-TRACTION DEVICE?

The FDA product code for BOGER AUTO-TRACTION DEVICE is ILZ.

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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.

K921711FLEXION DISTRATION SUPPORTAltoona Medical SupplyK895382VIBRA-TRAC TRACTION TABLEVibra-Trac IndustriesK884340AMX-110, AMX-II AND AMX-IIIDyna-MedK852398VECTOR BAR SUSPENSION/TRACTION UNITPowlan Manufacturing Co.K844490TRACTION ACCESSORIESJerome MedicalK831135SAUNDERS #7080 CERVICAL TRACTION SYSChattanooga Group, 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.

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