ERBOTOM ACC 450

FDA 510(k) Premarket Notification · Submission K896055 · Applicant: Erbe Electromedizin GmbH

Public Record 510(k) Submission Decision Date: 1990-02-13 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K896055.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K896055
Applicant / Sponsor
Device Name
ERBOTOM ACC 450
Product Code
GEI
Decision Date
1990-02-13
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
General, Plastic Surgery (SU)
Clearance Type
Traditional
Third Party Flag
N
Date Received
1989-10-18

Related Establishments / Registrations

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