BUTTERFLY NEEDLE ASSEMBLY

FDA 510(k) Premarket Notification · Submission K812404 · Applicant: Nu Tech Medical Systems

Public Record 510(k) Submission Decision Date: 1981-09-09 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K812404.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K812404
Applicant / Sponsor
Device Name
BUTTERFLY NEEDLE ASSEMBLY
Product Code
FMI
Decision Date
1981-09-09
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
General Hospital (HO)
Clearance Type
Traditional
Third Party Flag
N
Date Received
1981-08-20

Related Establishments / Registrations

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