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FDA 510(k)

BIPOLARD POLYPECTOMY SYSTEM (TM)

K-Number: K901302 · 1990-06-06

ApplicantMedical Devices, Inc.
Decision Date1990-06-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BIPOLARD POLYPECTOMY SYSTEM (TM) is the device name listed in this FDA 510(k) record. The listed applicant is Medical Devices, Inc.. It received FDA 510(k) clearance on 1990-06-06 under 510(k) number K901302. 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 BIPOLARD POLYPECTOMY SYSTEM (TM)?

BIPOLARD POLYPECTOMY SYSTEM (TM) is a medical device that received FDA 510(k) clearance on 1990-06-06. The listed applicant is Medical Devices, Inc.. The 510(k) number is K901302.

When did BIPOLARD POLYPECTOMY SYSTEM (TM) receive FDA 510(k) clearance?

BIPOLARD POLYPECTOMY SYSTEM (TM) received FDA 510(k) clearance on 1990-06-06, under 510(k) number K901302.

Who is the listed applicant for BIPOLARD POLYPECTOMY SYSTEM (TM)?

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

What is the FDA product code for BIPOLARD POLYPECTOMY SYSTEM (TM)?

The FDA product code for BIPOLARD POLYPECTOMY SYSTEM (TM) is GEI.

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Other records listing Medical Devices, Inc. as applicant

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Related Devices (Code: 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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