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FDA 510(k)

MODEL 2144.00 COMBINATION ENDO-SURGICAL DEVICE

K-Number: K910716 · 1991-04-16

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1991-04-16
Product CodeFCX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODEL 2144.00 COMBINATION ENDO-SURGICAL DEVICE 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 1991-04-16 under 510(k) number K910716. The device is classified under product code FCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 2144.00 COMBINATION ENDO-SURGICAL DEVICE?

MODEL 2144.00 COMBINATION ENDO-SURGICAL DEVICE is a medical device that received FDA 510(k) clearance on 1991-04-16. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K910716.

When did MODEL 2144.00 COMBINATION ENDO-SURGICAL DEVICE receive FDA 510(k) clearance?

MODEL 2144.00 COMBINATION ENDO-SURGICAL DEVICE received FDA 510(k) clearance on 1991-04-16, under 510(k) number K910716.

Who is the listed applicant for MODEL 2144.00 COMBINATION ENDO-SURGICAL DEVICE?

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 MODEL 2144.00 COMBINATION ENDO-SURGICAL DEVICE?

The FDA product code for MODEL 2144.00 COMBINATION ENDO-SURGICAL DEVICE is FCX.

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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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