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FDA 510(k)

TRAY AND BAG, CATHETERIZATION

K-Number: K790271 · 1979-03-06

ApplicantSnyder Laboratories, Inc.
Decision Date1979-03-06
Product CodeFCM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TRAY AND BAG, CATHETERIZATION is the device name listed in this FDA 510(k) record. The listed applicant is Snyder Laboratories, Inc.. It received FDA 510(k) clearance on 1979-03-06 under 510(k) number K790271. The device is classified under product code FCM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAY AND BAG, CATHETERIZATION?

TRAY AND BAG, CATHETERIZATION is a medical device that received FDA 510(k) clearance on 1979-03-06. The listed applicant is Snyder Laboratories, Inc.. The 510(k) number is K790271.

When did TRAY AND BAG, CATHETERIZATION receive FDA 510(k) clearance?

TRAY AND BAG, CATHETERIZATION received FDA 510(k) clearance on 1979-03-06, under 510(k) number K790271.

Who is the listed applicant for TRAY AND BAG, CATHETERIZATION?

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

What is the FDA product code for TRAY AND BAG, CATHETERIZATION?

The FDA product code for TRAY AND BAG, CATHETERIZATION is FCM.

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Related Devices (Code: FCM)

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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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