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FDA 510(k)

GRASPERS & SCISSORS (MINIMAL ACCESS SURG INSTR)

K-Number: K924469 · 1993-04-07

ApplicantConmedcorp
Decision Date1993-04-07
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GRASPERS & SCISSORS (MINIMAL ACCESS SURG INSTR) is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1993-04-07 under 510(k) number K924469. 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 GRASPERS & SCISSORS (MINIMAL ACCESS SURG INSTR)?

GRASPERS & SCISSORS (MINIMAL ACCESS SURG INSTR) is a medical device that received FDA 510(k) clearance on 1993-04-07. The listed applicant is Conmedcorp. The 510(k) number is K924469.

When did GRASPERS & SCISSORS (MINIMAL ACCESS SURG INSTR) receive FDA 510(k) clearance?

GRASPERS & SCISSORS (MINIMAL ACCESS SURG INSTR) received FDA 510(k) clearance on 1993-04-07, under 510(k) number K924469.

Who is the listed applicant for GRASPERS & SCISSORS (MINIMAL ACCESS SURG INSTR)?

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

What is the FDA product code for GRASPERS & SCISSORS (MINIMAL ACCESS SURG INSTR)?

The FDA product code for GRASPERS & SCISSORS (MINIMAL ACCESS SURG INSTR) is GEI.

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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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