Perimeter Mediastinal Drain

FDA 510(k) K844925 · Perimeter Medical, Inc.

Substantially Equivalent

510(k) numberK844925

Submission

Device name
Perimeter Mediastinal Drain
Applicant
Perimeter Medical, Inc.
Tucson, AZ, US
Received
December 19, 1984
Decision date
March 18, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

More from Perimeter Medical, Inc.

510(k)DeviceDecision
K844924Perimeter Yankauer Suction Tips & Sets · Traditional 03/18/1985SE
K844923Perimeter Sump Drain · Traditional 03/18/1985SE
K844922Perimeter Thoracic CatheterGBX · Traditional 03/18/1985SE
K844921Perimeter Closed Wound ResevoirGCY · Traditional 03/18/1985SE

Questions and answers

When was Perimeter Mediastinal Drain cleared by the FDA?

Perimeter Mediastinal Drain (K844925) received a 510(k) decision of Substantially Equivalent on March 18, 1985, 89 days after the submission was received.