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FDA 510(k)

KEYMED MOBILE ENDOSCOPY PATIENT COUCH

K-Number: K840920 · 1984-03-19

ApplicantKeymed, Inc.
Decision Date1984-03-19
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

KEYMED MOBILE ENDOSCOPY 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 1984-03-19 under 510(k) number K840920. 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 KEYMED MOBILE ENDOSCOPY PATIENT COUCH?

KEYMED MOBILE ENDOSCOPY PATIENT COUCH is a medical device that received FDA 510(k) clearance on 1984-03-19. The listed applicant is Keymed, Inc.. The 510(k) number is K840920.

When did KEYMED MOBILE ENDOSCOPY PATIENT COUCH receive FDA 510(k) clearance?

KEYMED MOBILE ENDOSCOPY PATIENT COUCH received FDA 510(k) clearance on 1984-03-19, under 510(k) number K840920.

Who is the listed applicant for KEYMED MOBILE ENDOSCOPY 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 KEYMED MOBILE ENDOSCOPY PATIENT COUCH?

The FDA product code for KEYMED MOBILE ENDOSCOPY 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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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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