Aneroid Sphygmometer

FDA 510(k) K771502 · Swartz Medical Equipment

Substantially Equivalent

510(k) numberK771502

Submission

Device name
Aneroid Sphygmometer
Applicant
Swartz Medical Equipment
Mchenry, IL, US
Received
August 5, 1977
Decision date
August 30, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

More from Swartz Medical Equipment

510(k)DeviceDecision
K771501Aneroid SphygmometerDXQ · Traditional 08/30/1977SE
K771581Stethoscope, Nursescope TypeDQD · Traditional 08/26/1977SE
K771506StethoscopeDQD · Traditional 08/26/1977SE
K771505StethoscopeDQD · Traditional 08/26/1977SE
K771504StethoscopeDQD · Traditional 08/26/1977SE

Questions and answers

When was Aneroid Sphygmometer cleared by the FDA?

Aneroid Sphygmometer (K771502) received a 510(k) decision of Substantially Equivalent on August 30, 1977, 25 days after the submission was received.