FDA 510(k) Premarket Notification K951256: DETACHABLE PLATINUM COIL (GUGLIELMI DETACHABLE COIL, GDC)

Submission Details & Decision

Normalized public record details for 510(k) notification K951256.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K951256

Applicant / Sponsor

Target Therapeutics

Device Name

DETACHABLE PLATINUM COIL (GUGLIELMI DETACHABLE COIL, GDC)

Product Code

HCG

Decision Date

1995-09-08

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Neurology (NE)

Clearance Type

Traditional

Third Party Flag

Date Received

1995-03-21

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