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FDA 510(k)

FLEXIBLE CHOLEDOCHOSCOPE/NEPHROSCOPE

K-Number: K810503 · 1981-04-03

ApplicantOlympus Corp.
Decision Date1981-04-03
Product CodeNWS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE CHOLEDOCHOSCOPE/NEPHROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1981-04-03 under 510(k) number K810503. The device is classified under product code NWS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIBLE CHOLEDOCHOSCOPE/NEPHROSCOPE?

FLEXIBLE CHOLEDOCHOSCOPE/NEPHROSCOPE is a medical device that received FDA 510(k) clearance on 1981-04-03. The listed applicant is Olympus Corp.. The 510(k) number is K810503.

When did FLEXIBLE CHOLEDOCHOSCOPE/NEPHROSCOPE receive FDA 510(k) clearance?

FLEXIBLE CHOLEDOCHOSCOPE/NEPHROSCOPE received FDA 510(k) clearance on 1981-04-03, under 510(k) number K810503.

Who is the listed applicant for FLEXIBLE CHOLEDOCHOSCOPE/NEPHROSCOPE?

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

What is the FDA product code for FLEXIBLE CHOLEDOCHOSCOPE/NEPHROSCOPE?

The FDA product code for FLEXIBLE CHOLEDOCHOSCOPE/NEPHROSCOPE is NWS.

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Other records listing Olympus 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.

K915402EW-10 AND EW-20K933200OLYMPUS PBD STENTSK942338OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIESK931763HF-RESECTION ELECTRODE, LOOP W/RUNNER ENDOS/ACCESSK934835FLOVALK931764HF RESECTION ELECTRODE, LOOP W/RUNNER HYSTER/ACCES

View all 142 devices →

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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