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FDA 510(k)

MCINTOSH, MILLER, FOREGGER BABY

K-Number: K945425 · 1995-03-20

ApplicantRudolf Riester GmbH & Co. KG
Decision Date1995-03-20
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MCINTOSH, MILLER, FOREGGER BABY is the device name listed in this FDA 510(k) record. The listed applicant is Rudolf Riester GmbH & Co. KG. It received FDA 510(k) clearance on 1995-03-20 under 510(k) number K945425. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MCINTOSH, MILLER, FOREGGER BABY?

MCINTOSH, MILLER, FOREGGER BABY is a medical device that received FDA 510(k) clearance on 1995-03-20. The listed applicant is Rudolf Riester GmbH & Co. KG. The 510(k) number is K945425.

When did MCINTOSH, MILLER, FOREGGER BABY receive FDA 510(k) clearance?

MCINTOSH, MILLER, FOREGGER BABY received FDA 510(k) clearance on 1995-03-20, under 510(k) number K945425.

Who is the listed applicant for MCINTOSH, MILLER, FOREGGER BABY?

The FDA 510(k) record lists Rudolf Riester GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MCINTOSH, MILLER, FOREGGER BABY?

The FDA product code for MCINTOSH, MILLER, FOREGGER BABY is CCW.

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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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