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FDA 510(k)

CAM 4 THERMOELECTRIC CHILD/ADULT MIST TENT

K-Number: K941547 · 1995-03-01

Decision Date1995-03-01
Product CodeBYK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CAM 4 THERMOELECTRIC CHILD/ADULT MIST TENT 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 1995-03-01 under 510(k) number K941547. The device is classified under product code BYK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAM 4 THERMOELECTRIC CHILD/ADULT MIST TENT?

CAM 4 THERMOELECTRIC CHILD/ADULT MIST TENT is a medical device that received FDA 510(k) clearance on 1995-03-01. The listed applicant is Allied Healthcare Products, Inc.. The 510(k) number is K941547.

When did CAM 4 THERMOELECTRIC CHILD/ADULT MIST TENT receive FDA 510(k) clearance?

CAM 4 THERMOELECTRIC CHILD/ADULT MIST TENT received FDA 510(k) clearance on 1995-03-01, under 510(k) number K941547.

Who is the listed applicant for CAM 4 THERMOELECTRIC CHILD/ADULT MIST TENT?

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 CAM 4 THERMOELECTRIC CHILD/ADULT MIST TENT?

The FDA product code for CAM 4 THERMOELECTRIC CHILD/ADULT MIST TENT is BYK.

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: BYK)

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

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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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