FDA 510(k) Premarket Notification K810767: RPMI 1640 MEDIUM

Submission Details & Decision

Normalized public record details for 510(k) notification K810767.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K810767

Applicant / Sponsor

Dutchland Laboratories, Inc.

Device Name

RPMI 1640 MEDIUM

Product Code

KIT

Decision Date

1981-05-08

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Hematology (HE)

Clearance Type

Traditional

Third Party Flag

Date Received

1981-03-23

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