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FDA 510(k)

VICTOREEN MODEL 530

K-Number: K931927 · 1993-11-15

ApplicantVictoreen, Inc.
Decision Date1993-11-15
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VICTOREEN MODEL 530 is the device name listed in this FDA 510(k) record. The listed applicant is Victoreen, Inc.. It received FDA 510(k) clearance on 1993-11-15 under 510(k) number K931927. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VICTOREEN MODEL 530?

VICTOREEN MODEL 530 is a medical device that received FDA 510(k) clearance on 1993-11-15. The listed applicant is Victoreen, Inc.. The 510(k) number is K931927.

When did VICTOREEN MODEL 530 receive FDA 510(k) clearance?

VICTOREEN MODEL 530 received FDA 510(k) clearance on 1993-11-15, under 510(k) number K931927.

Who is the listed applicant for VICTOREEN MODEL 530?

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 VICTOREEN MODEL 530?

The FDA product code for VICTOREEN MODEL 530 is IYE.

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Other records listing Victoreen, Inc. as applicant

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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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