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FDA 510(k)

FLO-PHORESIS - DESENSITIZER

K-Number: K844989 · 1985-04-01

ApplicantEastco, Inc.
Decision Date1985-04-01
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLO-PHORESIS - DESENSITIZER is the device name listed in this FDA 510(k) record. The listed applicant is Eastco, Inc.. It received FDA 510(k) clearance on 1985-04-01 under 510(k) number K844989. The device is classified under product code EGS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLO-PHORESIS - DESENSITIZER?

FLO-PHORESIS - DESENSITIZER is a medical device that received FDA 510(k) clearance on 1985-04-01. The listed applicant is Eastco, Inc.. The 510(k) number is K844989.

When did FLO-PHORESIS - DESENSITIZER receive FDA 510(k) clearance?

FLO-PHORESIS - DESENSITIZER received FDA 510(k) clearance on 1985-04-01, under 510(k) number K844989.

Who is the listed applicant for FLO-PHORESIS - DESENSITIZER?

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

What is the FDA product code for FLO-PHORESIS - DESENSITIZER?

The FDA product code for FLO-PHORESIS - DESENSITIZER is EGS.

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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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