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FDA 510(k)

THE KEYMED VARI-HEIGHT PATIENT COUCH

K-Number: K853421 · 1985-09-19

ApplicantKeymed, Inc.
Decision Date1985-09-19
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE KEYMED VARI-HEIGHT PATIENT COUCH is the device name listed in this FDA 510(k) record. The listed applicant is Keymed, Inc.. It received FDA 510(k) clearance on 1985-09-19 under 510(k) number K853421. 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 THE KEYMED VARI-HEIGHT PATIENT COUCH?

THE KEYMED VARI-HEIGHT PATIENT COUCH is a medical device that received FDA 510(k) clearance on 1985-09-19. The listed applicant is Keymed, Inc.. The 510(k) number is K853421.

When did THE KEYMED VARI-HEIGHT PATIENT COUCH receive FDA 510(k) clearance?

THE KEYMED VARI-HEIGHT PATIENT COUCH received FDA 510(k) clearance on 1985-09-19, under 510(k) number K853421.

Who is the listed applicant for THE KEYMED VARI-HEIGHT PATIENT COUCH?

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

What is the FDA product code for THE KEYMED VARI-HEIGHT PATIENT COUCH?

The FDA product code for THE KEYMED VARI-HEIGHT PATIENT COUCH is FPO.

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Other records listing Keymed, Inc. as applicant

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K100803OLYMPUS FLUSHING PUMP OFP MODEL: OFP-1K921179OLYMPUS-KEYMED DISINFECTANT FUME EXTRACTOR DFE-20K881004OLYMPUS-KEYMED ENDOSCOPIC CO2 REGULATOR, MODEL ECRK861821KEYMED FIBERSCOPE AUTO DISINFECTORK864801THE KEYMED HI-LIGHT 250 LIGHT SOURCEK862000KEYMED FLEXIBLE ESOPHAGEAL DILATORS

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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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