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FDA 510(k)

FLEXIBLE FIBEROPTIC ENDOSCOPE

K-Number: K850393 · 1985-06-04

ApplicantMicrovasive
Decision Date1985-06-04
Product Code
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE FIBEROPTIC ENDOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Microvasive. It received FDA 510(k) clearance on 1985-06-04 under 510(k) number K850393. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIBLE FIBEROPTIC ENDOSCOPE?

FLEXIBLE FIBEROPTIC ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1985-06-04. The listed applicant is Microvasive. The 510(k) number is K850393.

When did FLEXIBLE FIBEROPTIC ENDOSCOPE receive FDA 510(k) clearance?

FLEXIBLE FIBEROPTIC ENDOSCOPE received FDA 510(k) clearance on 1985-06-04, under 510(k) number K850393.

Who is the listed applicant for FLEXIBLE FIBEROPTIC ENDOSCOPE?

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

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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

View all 18 devices →

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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