Medical Device Manufacturer · US , Mchenry , IL

Mem Medical, Inc. - FDA 510(k) Cleared Devices

27 submissions · 27 cleared · Since 1979

Total

Cleared

Denied

Mem Medical, Inc. has 27 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.

Historical record: 27 cleared submissions from 1979 to 1979.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Mem Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Mem Medical, Inc.

27 devices

1-12 of 27

Cleared Oct 09, 1979

IMV W/BAG & HOSES #M-509

K791904 · CBO

Anesthesiology · 14d

Cleared Oct 09, 1979

IMV W/BAG & TUBING #M-508

RETARD VALVE 3-STACK #M-515

K791907 · CBP

Anesthesiology · 14d

Cleared Oct 09, 1979

RETARD VALVE 3-STACK #M-514

THREE LITER BAG #M-512

IMV FOR MONITORING #M-510

RESPIROMETER MANIFOLD M-505

K791848 · BYX

Anesthesiology · 12d

Cleared Oct 01, 1979

ONE-WAY VALVE-MALE, M-504

K791849 · CBP

Anesthesiology · 12d

Mem Medical, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Mem Medical, Inc.

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