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FDA 510(k)

RIGID FIBEROPITC ENDOSCOPE

K-Number: K844769 · 1985-01-15

ApplicantMicrovasive
Decision Date1985-01-15
Product CodeGCM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RIGID FIBEROPITC ENDOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Microvasive. It received FDA 510(k) clearance on 1985-01-15 under 510(k) number K844769. The device is classified under product code GCM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIGID FIBEROPITC ENDOSCOPE?

RIGID FIBEROPITC ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1985-01-15. The listed applicant is Microvasive. The 510(k) number is K844769.

When did RIGID FIBEROPITC ENDOSCOPE receive FDA 510(k) clearance?

RIGID FIBEROPITC ENDOSCOPE received FDA 510(k) clearance on 1985-01-15, under 510(k) number K844769.

Who is the listed applicant for RIGID FIBEROPITC ENDOSCOPE?

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

What is the FDA product code for RIGID FIBEROPITC ENDOSCOPE?

The FDA product code for RIGID FIBEROPITC ENDOSCOPE is GCM.

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 Microvasive 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.

K872771LOW PROFILE GASTROSTOMYK870705THERMAL COAGULATORK861323REPLACEMENT GASTROSTOMY TUBEK861309JEJUNAL FEEDING TUBEK860589INFLATOR/DEFLATOR PISTON SYRINGEK860366CHALLENGER HOT BIOPSY FORCEPS

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Related Devices (Code: GCM)

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.

K203226TELESCOPE 0 O 10MM WL 305MM / TELESCOPE 30 O 10MM WL 305MM / TELESCOPE 50 O 10MM WL 305MM, TELESCOPE 0 O 10MM WL 440MM / TELESCOPE 30 O 10MM WL 440MM / TELESCOPE 50 O 10MM WL 440MMRichard Wolf Medical Instruments CorporationK083840MSI MEDSERV INTERNATIONAL-RIGID ENDOSCOPEMsi Medserv International Deutschland GmbHK001217INSIDE VIEWMonadnock Optics, Inc.K993103ENDOSCOPES,10MM DIAMETER 0 DEGREES; ENDOSCOPES, 10MM DIAMETER, 30 DEGREES; ENDOSCOPES, 10MM DIAMETER, 50 DEGREESRichard Wolf Medical Instruments Corp.K993445OMNISONIC ENDOSCOPIC DEFLECTOROmnisonics Medical TechnologiesK962393KSEA SET FOR ENDOSCOPIC ASSISTED INTUBATIONKARL STORZ Endoscopy-America, 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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