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FDA 510(k)

RID-DECUBE II

K-Number: K965207 · 1997-08-21

Decision Date1997-08-21
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RID-DECUBE II is the device name listed in this FDA 510(k) record. The listed applicant is Skin Care Management, Inc.. It received FDA 510(k) clearance on 1997-08-21 under 510(k) number K965207. The device is classified under product code FNM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RID-DECUBE II?

RID-DECUBE II is a medical device that received FDA 510(k) clearance on 1997-08-21. The listed applicant is Skin Care Management, Inc.. The 510(k) number is K965207.

When did RID-DECUBE II receive FDA 510(k) clearance?

RID-DECUBE II received FDA 510(k) clearance on 1997-08-21, under 510(k) number K965207.

Who is the listed applicant for RID-DECUBE II?

The FDA 510(k) record lists Skin Care Management, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RID-DECUBE II?

The FDA product code for RID-DECUBE II is FNM.

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.

Related Devices (Code: FNM)

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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