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FDA 510(k)

ENDOSCOPIC DELIVERY SYSTEM

K-Number: K913172 · 1991-09-06

ApplicantMedco Products, Co., Inc.
Decision Date1991-09-06
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medco Products, Co., Inc.. It received FDA 510(k) clearance on 1991-09-06 under 510(k) number K913172. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPIC DELIVERY SYSTEM?

ENDOSCOPIC DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 1991-09-06. The listed applicant is Medco Products, Co., Inc.. The 510(k) number is K913172.

When did ENDOSCOPIC DELIVERY SYSTEM receive FDA 510(k) clearance?

ENDOSCOPIC DELIVERY SYSTEM received FDA 510(k) clearance on 1991-09-06, under 510(k) number K913172.

Who is the listed applicant for ENDOSCOPIC DELIVERY SYSTEM?

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

What is the FDA product code for ENDOSCOPIC DELIVERY SYSTEM?

The FDA product code for ENDOSCOPIC DELIVERY SYSTEM is GCJ.

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Other records listing Medco Products, Co., Inc. as applicant

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Related Devices (Code: GCJ)

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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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