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FDA 510(k)

IMAG, IPOD, EZ-FIND AND ISLIDE

K-Number: K090362 · 2009-02-27

ApplicantVoguestrap
Decision Date2009-02-27
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

IMAG, IPOD, EZ-FIND AND ISLIDE is the device name listed in this FDA 510(k) record. The listed applicant is Voguestrap. It received FDA 510(k) clearance on 2009-02-27 under 510(k) number K090362. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMAG, IPOD, EZ-FIND AND ISLIDE?

IMAG, IPOD, EZ-FIND AND ISLIDE is a medical device that received FDA 510(k) clearance on 2009-02-27. The listed applicant is Voguestrap. The 510(k) number is K090362.

When did IMAG, IPOD, EZ-FIND AND ISLIDE receive FDA 510(k) clearance?

IMAG, IPOD, EZ-FIND AND ISLIDE received FDA 510(k) clearance on 2009-02-27, under 510(k) number K090362.

Who is the listed applicant for IMAG, IPOD, EZ-FIND AND ISLIDE?

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

What is the FDA product code for IMAG, IPOD, EZ-FIND AND ISLIDE?

The FDA product code for IMAG, IPOD, EZ-FIND AND ISLIDE is LRX.

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Official Source

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