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FDA 510(k)

ALL-VUE & GAMMA-VUE VIAL SHIELDS

K-Number: K934548 · 1993-11-12

ApplicantVictoreen, Inc.
Decision Date1993-11-12
Product CodeIWW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ALL-VUE & GAMMA-VUE VIAL SHIELDS is the device name listed in this FDA 510(k) record. The listed applicant is Victoreen, Inc.. It received FDA 510(k) clearance on 1993-11-12 under 510(k) number K934548. The device is classified under product code IWW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALL-VUE & GAMMA-VUE VIAL SHIELDS?

ALL-VUE & GAMMA-VUE VIAL SHIELDS is a medical device that received FDA 510(k) clearance on 1993-11-12. The listed applicant is Victoreen, Inc.. The 510(k) number is K934548.

When did ALL-VUE & GAMMA-VUE VIAL SHIELDS receive FDA 510(k) clearance?

ALL-VUE & GAMMA-VUE VIAL SHIELDS received FDA 510(k) clearance on 1993-11-12, under 510(k) number K934548.

Who is the listed applicant for ALL-VUE & GAMMA-VUE VIAL SHIELDS?

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

What is the FDA product code for ALL-VUE & GAMMA-VUE VIAL SHIELDS?

The FDA product code for ALL-VUE & GAMMA-VUE VIAL SHIELDS is IWW.

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Other records listing Victoreen, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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