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FDA 510(k)

MEDICAL MAGGOTS, CREATURE COMFORTS

K-Number: K072438 · 2007-10-05

Decision Date2007-10-05
Product CodeNQK
DecisionSubstantially Equivalent

Device Summary

MEDICAL MAGGOTS, CREATURE COMFORTS is the device name listed in this FDA 510(k) record. The listed applicant is Monarch Labs, LLC. It received FDA 510(k) clearance on 2007-10-05 under 510(k) number K072438. The device is classified under product code NQK. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICAL MAGGOTS, CREATURE COMFORTS?

MEDICAL MAGGOTS, CREATURE COMFORTS is a medical device that received FDA 510(k) clearance on 2007-10-05. The listed applicant is Monarch Labs, LLC. The 510(k) number is K072438.

When did MEDICAL MAGGOTS, CREATURE COMFORTS receive FDA 510(k) clearance?

MEDICAL MAGGOTS, CREATURE COMFORTS received FDA 510(k) clearance on 2007-10-05, under 510(k) number K072438.

Who is the listed applicant for MEDICAL MAGGOTS, CREATURE COMFORTS?

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

What is the FDA product code for MEDICAL MAGGOTS, CREATURE COMFORTS?

The FDA product code for MEDICAL MAGGOTS, CREATURE COMFORTS is NQK.

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 Monarch Labs, LLC 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.

Related Devices (Code: NQK)

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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