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FDA 510(k)

MODIFICATION TO: PRONTO DRY

K-Number: K002451 · 2000-09-29

ApplicantMedical Instruments Corporation, AG
Decision Date2000-09-29
Product CodeLYR
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO: PRONTO DRY is the device name listed in this FDA 510(k) record. The listed applicant is Medical Instruments Corporation, AG. It received FDA 510(k) clearance on 2000-09-29 under 510(k) number K002451. The device is classified under product code LYR. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO: PRONTO DRY?

MODIFICATION TO: PRONTO DRY is a medical device that received FDA 510(k) clearance on 2000-09-29. The listed applicant is Medical Instruments Corporation, AG. The 510(k) number is K002451.

When did MODIFICATION TO: PRONTO DRY receive FDA 510(k) clearance?

MODIFICATION TO: PRONTO DRY received FDA 510(k) clearance on 2000-09-29, under 510(k) number K002451.

Who is the listed applicant for MODIFICATION TO: PRONTO DRY?

The FDA 510(k) record lists Medical Instruments Corporation, AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION TO: PRONTO DRY?

The FDA product code for MODIFICATION TO: PRONTO DRY is LYR.

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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.

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