FDA 510(k)

MORCE SCOPE SET 8970 WITH POWER CONTROL 2303 AND SUCTION PUMP 2207

K-Number: K041610 · 2004-08-19

ApplicantRichard Wolf Medical Instruments Corp.

Decision Date2004-08-19

Product CodeFJL

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MORCE SCOPE SET 8970 WITH POWER CONTROL 2303 AND SUCTION PUMP 2207 is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 2004-08-19 under 510(k) number K041610. The device is classified under product code FJL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MORCE SCOPE SET 8970 WITH POWER CONTROL 2303 AND SUCTION PUMP 2207?

MORCE SCOPE SET 8970 WITH POWER CONTROL 2303 AND SUCTION PUMP 2207 is a medical device that received FDA 510(k) clearance on 2004-08-19. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K041610.

When did MORCE SCOPE SET 8970 WITH POWER CONTROL 2303 AND SUCTION PUMP 2207 receive FDA 510(k) clearance?

MORCE SCOPE SET 8970 WITH POWER CONTROL 2303 AND SUCTION PUMP 2207 received FDA 510(k) clearance on 2004-08-19, under 510(k) number K041610.

Who is the listed applicant for MORCE SCOPE SET 8970 WITH POWER CONTROL 2303 AND SUCTION PUMP 2207?

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

What is the FDA product code for MORCE SCOPE SET 8970 WITH POWER CONTROL 2303 AND SUCTION PUMP 2207?

The FDA product code for MORCE SCOPE SET 8970 WITH POWER CONTROL 2303 AND SUCTION PUMP 2207 is FJL.

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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.