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FDA 510(k)

OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIES

K-Number: K942338 · 1994-11-30

ApplicantOlympus Corp.
Decision Date1994-11-30
Product CodeFDT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1994-11-30 under 510(k) number K942338. The device is classified under product code FDT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIES?

OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1994-11-30. The listed applicant is Olympus Corp.. The 510(k) number is K942338.

When did OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIES receive FDA 510(k) clearance?

OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIES received FDA 510(k) clearance on 1994-11-30, under 510(k) number K942338.

Who is the listed applicant for OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIES?

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 OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIES?

The FDA product code for OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIES is FDT.

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Related Devices (Code: FDT)

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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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