FDA 510(k)

RACK-IT (R)

K-Number: K903096 · 1990-10-01

Decision Date1990-10-01

Product CodeFLE

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

RACK-IT (R) is the device name listed in this FDA 510(k) record. The listed applicant is Vengo Industries, Inc.. It received FDA 510(k) clearance on 1990-10-01 under 510(k) number K903096. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RACK-IT (R)?

RACK-IT (R) is a medical device that received FDA 510(k) clearance on 1990-10-01. The listed applicant is Vengo Industries, Inc.. The 510(k) number is K903096.

When did RACK-IT (R) receive FDA 510(k) clearance?

RACK-IT (R) received FDA 510(k) clearance on 1990-10-01, under 510(k) number K903096.

Who is the listed applicant for RACK-IT (R)?

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

What is the FDA product code for RACK-IT (R)?

The FDA product code for RACK-IT (R) is FLE.

Related Devices (Code: FLE)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.