FDA 510(k) Premarket Notification K834189: JAKOBI SURG. INSTRUMENTS #7 44/47

Submission Details & Decision

Normalized public record details for 510(k) notification K834189.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K834189

Applicant / Sponsor

Imm Enterprises , Ltd.

Device Name

JAKOBI SURG. INSTRUMENTS #7 44/47

Product Code

EPY

Decision Date

1984-03-06

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

General, Plastic Surgery (SU)

Clearance Type

Traditional

Third Party Flag

Date Received

1983-11-21

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