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FDA 510(k)

SCHUCO MIST AND SCHUCO DELUXE MIST

K-Number: K051260 · 2005-09-15

Decision Date2005-09-15
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SCHUCO MIST AND SCHUCO DELUXE MIST is the device name listed in this FDA 510(k) record. The listed applicant is Allied Healthcare Products, Inc.. It received FDA 510(k) clearance on 2005-09-15 under 510(k) number K051260. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCHUCO MIST AND SCHUCO DELUXE MIST?

SCHUCO MIST AND SCHUCO DELUXE MIST is a medical device that received FDA 510(k) clearance on 2005-09-15. The listed applicant is Allied Healthcare Products, Inc.. The 510(k) number is K051260.

When did SCHUCO MIST AND SCHUCO DELUXE MIST receive FDA 510(k) clearance?

SCHUCO MIST AND SCHUCO DELUXE MIST received FDA 510(k) clearance on 2005-09-15, under 510(k) number K051260.

Who is the listed applicant for SCHUCO MIST AND SCHUCO DELUXE MIST?

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

What is the FDA product code for SCHUCO MIST AND SCHUCO DELUXE MIST?

The FDA product code for SCHUCO MIST AND SCHUCO DELUXE MIST is CAF.

Related Clinical Trials

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.

Other records listing Allied Healthcare Products, Inc. as applicant

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.

View all 24 devices →

Related Devices (Code: CAF)

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.

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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