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FDA 510(k)

KENDRICK EXTRICATION DEVICE

K-Number: K781761 · 1978-10-27

ApplicantMedi-Ked, Inc.
Decision Date1978-10-27
Product CodeIQF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KENDRICK EXTRICATION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Ked, Inc.. It received FDA 510(k) clearance on 1978-10-27 under 510(k) number K781761. The device is classified under product code IQF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KENDRICK EXTRICATION DEVICE?

KENDRICK EXTRICATION DEVICE is a medical device that received FDA 510(k) clearance on 1978-10-27. The listed applicant is Medi-Ked, Inc.. The 510(k) number is K781761.

When did KENDRICK EXTRICATION DEVICE receive FDA 510(k) clearance?

KENDRICK EXTRICATION DEVICE received FDA 510(k) clearance on 1978-10-27, under 510(k) number K781761.

Who is the listed applicant for KENDRICK EXTRICATION DEVICE?

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

What is the FDA product code for KENDRICK EXTRICATION DEVICE?

The FDA product code for KENDRICK EXTRICATION DEVICE is IQF.

Related Clinical Trials

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Related Devices (Code: IQF)

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.

K832741JASON CERVICAL ORTHOSISOrthomedicsK812342ZEE EXTRICATION DEVICEZee Medical Products Co., Inc.K811297CERVICAL SUPPORTOrthomedicsK810555SCOLIOSIS ORTHOTIC SYSTEMOrthomedicsK791350POPE AMBULATORY HALO VESTHospital Products Co.K780489SPINE BOARDMarullo, Baldwin, Frieden, Gatewood,

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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