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FDA 510(k)

FO18/FO98 SCRUBOFLEX SHOWERPROOF BRUSH MASSAGER

K-Number: K931636 · 1994-03-28

ApplicantFairform Mfg., Co., Ltd.
Decision Date1994-03-28
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FO18/FO98 SCRUBOFLEX SHOWERPROOF BRUSH MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Fairform Mfg., Co., Ltd.. It received FDA 510(k) clearance on 1994-03-28 under 510(k) number K931636. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FO18/FO98 SCRUBOFLEX SHOWERPROOF BRUSH MASSAGER?

FO18/FO98 SCRUBOFLEX SHOWERPROOF BRUSH MASSAGER is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Fairform Mfg., Co., Ltd.. The 510(k) number is K931636.

When did FO18/FO98 SCRUBOFLEX SHOWERPROOF BRUSH MASSAGER receive FDA 510(k) clearance?

FO18/FO98 SCRUBOFLEX SHOWERPROOF BRUSH MASSAGER received FDA 510(k) clearance on 1994-03-28, under 510(k) number K931636.

Who is the listed applicant for FO18/FO98 SCRUBOFLEX SHOWERPROOF BRUSH MASSAGER?

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

What is the FDA product code for FO18/FO98 SCRUBOFLEX SHOWERPROOF BRUSH MASSAGER?

The FDA product code for FO18/FO98 SCRUBOFLEX SHOWERPROOF BRUSH MASSAGER is ISA.

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Other records listing Fairform Mfg., Co., Ltd. as applicant

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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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