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FDA 510(k)

LIGHT DRAPE

K-Number: K043234 · 2005-05-25

Decision Date2005-05-25
Product CodeMMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIGHT DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Wrapped IN Comfort. It received FDA 510(k) clearance on 2005-05-25 under 510(k) number K043234. The device is classified under product code MMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHT DRAPE?

LIGHT DRAPE is a medical device that received FDA 510(k) clearance on 2005-05-25. The listed applicant is Wrapped IN Comfort. The 510(k) number is K043234.

When did LIGHT DRAPE receive FDA 510(k) clearance?

LIGHT DRAPE received FDA 510(k) clearance on 2005-05-25, under 510(k) number K043234.

Who is the listed applicant for LIGHT DRAPE?

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

What is the FDA product code for LIGHT DRAPE?

The FDA product code for LIGHT DRAPE is MMP.

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 Wrapped IN Comfort 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: MMP)

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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