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FDA 510(k)

ELEC SURG INSTR FOR LOPPROSCOPE CHOLECYSTECYOMY

K-Number: K912968 · 1991-09-25

ApplicantPaden Foudry , Ltd.
Decision Date1991-09-25
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELEC SURG INSTR FOR LOPPROSCOPE CHOLECYSTECYOMY is the device name listed in this FDA 510(k) record. The listed applicant is Paden Foudry , Ltd.. It received FDA 510(k) clearance on 1991-09-25 under 510(k) number K912968. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELEC SURG INSTR FOR LOPPROSCOPE CHOLECYSTECYOMY?

ELEC SURG INSTR FOR LOPPROSCOPE CHOLECYSTECYOMY is a medical device that received FDA 510(k) clearance on 1991-09-25. The listed applicant is Paden Foudry , Ltd.. The 510(k) number is K912968.

When did ELEC SURG INSTR FOR LOPPROSCOPE CHOLECYSTECYOMY receive FDA 510(k) clearance?

ELEC SURG INSTR FOR LOPPROSCOPE CHOLECYSTECYOMY received FDA 510(k) clearance on 1991-09-25, under 510(k) number K912968.

Who is the listed applicant for ELEC SURG INSTR FOR LOPPROSCOPE CHOLECYSTECYOMY?

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

What is the FDA product code for ELEC SURG INSTR FOR LOPPROSCOPE CHOLECYSTECYOMY?

The FDA product code for ELEC SURG INSTR FOR LOPPROSCOPE CHOLECYSTECYOMY is GEI.

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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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