Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

REVLON RVSP3501 SPA MOISTURESTAY PARAFFIN BATH (TYPE SPB3752EA)

K-Number: K093100 · 2009-11-24

Decision Date2009-11-24
Product CodeIMC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

REVLON RVSP3501 SPA MOISTURESTAY PARAFFIN BATH (TYPE SPB3752EA) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Comfort Technology Co., Ltd.. It received FDA 510(k) clearance on 2009-11-24 under 510(k) number K093100. The device is classified under product code IMC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REVLON RVSP3501 SPA MOISTURESTAY PARAFFIN BATH (TYPE SPB3752EA)?

REVLON RVSP3501 SPA MOISTURESTAY PARAFFIN BATH (TYPE SPB3752EA) is a medical device that received FDA 510(k) clearance on 2009-11-24. The listed applicant is Shenzhen Comfort Technology Co., Ltd.. The 510(k) number is K093100.

When did REVLON RVSP3501 SPA MOISTURESTAY PARAFFIN BATH (TYPE SPB3752EA) receive FDA 510(k) clearance?

REVLON RVSP3501 SPA MOISTURESTAY PARAFFIN BATH (TYPE SPB3752EA) received FDA 510(k) clearance on 2009-11-24, under 510(k) number K093100.

Who is the listed applicant for REVLON RVSP3501 SPA MOISTURESTAY PARAFFIN BATH (TYPE SPB3752EA)?

The FDA 510(k) record lists Shenzhen Comfort Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REVLON RVSP3501 SPA MOISTURESTAY PARAFFIN BATH (TYPE SPB3752EA)?

The FDA product code for REVLON RVSP3501 SPA MOISTURESTAY PARAFFIN BATH (TYPE SPB3752EA) is IMC.

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: IMC)

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.

↑