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FDA 510(k)

HAND-CARRIED STRETCHERS/BREAK AWAY FLAT

K-Number: K904511 · 1990-10-12

ApplicantMinto Research & Development, Inc.
Decision Date1990-10-12
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HAND-CARRIED STRETCHERS/BREAK AWAY FLAT is the device name listed in this FDA 510(k) record. The listed applicant is Minto Research & Development, Inc.. It received FDA 510(k) clearance on 1990-10-12 under 510(k) number K904511. 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 HAND-CARRIED STRETCHERS/BREAK AWAY FLAT?

HAND-CARRIED STRETCHERS/BREAK AWAY FLAT is a medical device that received FDA 510(k) clearance on 1990-10-12. The listed applicant is Minto Research & Development, Inc.. The 510(k) number is K904511.

When did HAND-CARRIED STRETCHERS/BREAK AWAY FLAT receive FDA 510(k) clearance?

HAND-CARRIED STRETCHERS/BREAK AWAY FLAT received FDA 510(k) clearance on 1990-10-12, under 510(k) number K904511.

Who is the listed applicant for HAND-CARRIED STRETCHERS/BREAK AWAY FLAT?

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

What is the FDA product code for HAND-CARRIED STRETCHERS/BREAK AWAY FLAT?

The FDA product code for HAND-CARRIED STRETCHERS/BREAK AWAY FLAT is FPP.

Related Clinical Trials

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.

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Other records listing Minto Research & Development, Inc. as applicant

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.

K940590MINTO SKIN TRACTION MOTORK904723FORCEPSK904494HAND-CARRIED STRETCHERS

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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