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FDA 510(k)

MANHANDLER

K-Number: K905381 · 1991-03-13

ApplicantLifeport, Inc.
Decision Date1991-03-13
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MANHANDLER is the device name listed in this FDA 510(k) record. The listed applicant is Lifeport, Inc.. It received FDA 510(k) clearance on 1991-03-13 under 510(k) number K905381. 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 MANHANDLER?

MANHANDLER is a medical device that received FDA 510(k) clearance on 1991-03-13. The listed applicant is Lifeport, Inc.. The 510(k) number is K905381.

When did MANHANDLER receive FDA 510(k) clearance?

MANHANDLER received FDA 510(k) clearance on 1991-03-13, under 510(k) number K905381.

Who is the listed applicant for MANHANDLER?

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

What is the FDA product code for MANHANDLER?

The FDA product code for MANHANDLER 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

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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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