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FDA 510(k)

MODEL 561 C-ARM PROCEDURES STRETCHER

K-Number: K923730 · 1994-02-09

ApplicantMidmark Corp.
Decision Date1994-02-09
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 561 C-ARM PROCEDURES STRETCHER is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corp.. It received FDA 510(k) clearance on 1994-02-09 under 510(k) number K923730. The device is classified under product code FPO. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 561 C-ARM PROCEDURES STRETCHER?

MODEL 561 C-ARM PROCEDURES STRETCHER is a medical device that received FDA 510(k) clearance on 1994-02-09. The listed applicant is Midmark Corp.. The 510(k) number is K923730.

When did MODEL 561 C-ARM PROCEDURES STRETCHER receive FDA 510(k) clearance?

MODEL 561 C-ARM PROCEDURES STRETCHER received FDA 510(k) clearance on 1994-02-09, under 510(k) number K923730.

Who is the listed applicant for MODEL 561 C-ARM PROCEDURES STRETCHER?

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

What is the FDA product code for MODEL 561 C-ARM PROCEDURES STRETCHER?

The FDA product code for MODEL 561 C-ARM PROCEDURES STRETCHER is FPO.

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Other records listing Midmark Corp. 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.

K122643VANTAGE MODEL V5000, V5100, V5000C, V5100CK112380CLEARVISIONK090670MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZERK023348MIDMARK M9 ULTRACLAVE STEAM STERILIZERK003090MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEMK992744MIDMARK M4*9 EASYCLAVE STEAM STERILIZER

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Related Devices (Code: FPO)

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K113598POWER-LOAD COT FASTENER SYSTEMStryker MedicalK072598IRSG I-MOVER FOR BEDSInternational Retail Services Group, LLCK972528DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759)Dyna Corp.K955766ADULT-PEDIATRIC TRANSPORT SYSTEMInternational Biomedical, Inc.K962181HARE MODEL 2000 EZ LOADER MODEL 95555Dyna Corp.K961437WHEELED STRETCHERHill-Rom, 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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