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FDA 510(k)

PUMUCKL AND/OR DIETERLE

K-Number: K904037 · 1990-09-24

ApplicantPumuckl
Decision Date1990-09-24
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PUMUCKL AND/OR DIETERLE is the device name listed in this FDA 510(k) record. The listed applicant is Pumuckl. It received FDA 510(k) clearance on 1990-09-24 under 510(k) number K904037. The device is classified under product code HQZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PUMUCKL AND/OR DIETERLE?

PUMUCKL AND/OR DIETERLE is a medical device that received FDA 510(k) clearance on 1990-09-24. The listed applicant is Pumuckl. The 510(k) number is K904037.

When did PUMUCKL AND/OR DIETERLE receive FDA 510(k) clearance?

PUMUCKL AND/OR DIETERLE received FDA 510(k) clearance on 1990-09-24, under 510(k) number K904037.

Who is the listed applicant for PUMUCKL AND/OR DIETERLE?

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

What is the FDA product code for PUMUCKL AND/OR DIETERLE?

The FDA product code for PUMUCKL AND/OR DIETERLE is HQZ.

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Related Devices (Code: HQZ)

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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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