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FDA 510(k)

THE SMITHCOT

K-Number: K896261 · 1989-12-22

ApplicantRam Marketing, Inc.
Decision Date1989-12-22
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE SMITHCOT is the device name listed in this FDA 510(k) record. The listed applicant is Ram Marketing, Inc.. It received FDA 510(k) clearance on 1989-12-22 under 510(k) number K896261. The device is classified under product code FPP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE SMITHCOT?

THE SMITHCOT is a medical device that received FDA 510(k) clearance on 1989-12-22. The listed applicant is Ram Marketing, Inc.. The 510(k) number is K896261.

When did THE SMITHCOT receive FDA 510(k) clearance?

THE SMITHCOT received FDA 510(k) clearance on 1989-12-22, under 510(k) number K896261.

Who is the listed applicant for THE SMITHCOT?

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

What is the FDA product code for THE SMITHCOT?

The FDA product code for THE SMITHCOT is FPP.

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Related Devices (Code: FPP)

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.

K030283BABY PODPrism Enterprises, Inc.K942356MED-EVAC-4 MEDICAL EVACUATION STRETCHERMontery Bay Corp.K940130STRYKER MODEL 6110 EMERGENCY/POLE STRETCHERStryker Corp.K940245EVACU-SLEDEvacu Technologies, Inc.K924275RESTRAINING STRETCHERDmsK922816U P CUSTOM DESIGN, INC. COT EQUIPMENT CARRIERUp Custom Design, 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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