FDA 510(k) Premarket Notification K931629: CARAPACE ANGIOGRAPHY TRAYS

Submission Details & Decision

Normalized public record details for 510(k) notification K931629.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K931629

Applicant / Sponsor

Carapace, Inc.

Device Name

CARAPACE ANGIOGRAPHY TRAYS

Product Code

DQO

Decision Date

1993-12-06

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Cardiovascular (CV)

Clearance Type

Traditional

Third Party Flag

Date Received

1993-04-02

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