VESSA FLIVVA

FDA 510(k) Premarket Notification · Submission K853594 · Applicant: Vessa , Ltd.

Public Record 510(k) Submission Decision Date: 1985-09-24 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K853594.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K853594
Applicant / Sponsor
Device Name
VESSA FLIVVA
Product Code
ITI
Decision Date
1985-09-24
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Physical Medicine (PM)
Clearance Type
Traditional
Third Party Flag
N
Date Received
1985-08-27

Related Establishments / Registrations

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