Duran Flexible Ring

FDA 510(k) K780568 · Hancock Laboratories, Inc.

Substantially Equivalent

510(k) numberK780568

Submission

Device name
Duran Flexible Ring
Applicant
Hancock Laboratories, Inc.
Mchenry, IL, US
Received
April 10, 1978
Decision date
May 26, 1978
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

More from Hancock Laboratories, Inc.

510(k)DeviceDecision
K801885Hancock * ObturatorsDTI · Traditional 09/09/1980SE
K800703Modified Catheter PackageDQO · Traditional 04/08/1980SE
K800122Hancock Aortic PunchDWS · Traditional 02/01/1980SE
K790534Mersilene SuturesKRH · Traditional 03/26/1979SE

Questions and answers

When was Duran Flexible Ring cleared by the FDA?

Duran Flexible Ring (K780568) received a 510(k) decision of Substantially Equivalent on May 26, 1978, 46 days after the submission was received.