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FDA 510(k)

SPINE BOARD

K-Number: K780489 · 1978-04-12

ApplicantMarullo, Baldwin, Frieden, Gatewood,
Decision Date1978-04-12
Product CodeIQF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SPINE BOARD is the device name listed in this FDA 510(k) record. The listed applicant is Marullo, Baldwin, Frieden, Gatewood,. It received FDA 510(k) clearance on 1978-04-12 under 510(k) number K780489. 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 SPINE BOARD?

SPINE BOARD is a medical device that received FDA 510(k) clearance on 1978-04-12. The listed applicant is Marullo, Baldwin, Frieden, Gatewood,. The 510(k) number is K780489.

When did SPINE BOARD receive FDA 510(k) clearance?

SPINE BOARD received FDA 510(k) clearance on 1978-04-12, under 510(k) number K780489.

Who is the listed applicant for SPINE BOARD?

The FDA 510(k) record lists Marullo, Baldwin, Frieden, Gatewood, as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPINE BOARD?

The FDA product code for SPINE BOARD is IQF.

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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.K781761KENDRICK EXTRICATION DEVICEMedi-Ked, 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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