Medical Device Manufacturer · US , Mchenry , IL

Ndm Corp. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1976

Total

Cleared

Denied

Ndm Corp. has 11 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 11 cleared submissions from 1976 to 1993. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Ndm Corp. Filter by specialty or product code using the sidebar.

Ndm Corp. 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 - Ndm Corp.

11 devices

1-11 of 11

Cleared May 12, 1993

CLEARSITE STERILE WOUND DRESSING, NDM WOUND DRESSI

K926202 · NAE

General & Plastic Surgery · 154d

Cleared May 09, 1990

NDM SWITCHPEN HOLSTER

K901145 · GEI

General & Plastic Surgery · 58d

Cleared Nov 14, 1985

DIATEMP ELECTROSURGICAL PEN

K853968 · GEI

General & Plastic Surgery · 49d

NDM DIATEMP INFANT ELECTROSURG. DISP. P.

K810920 · HAM

General & Plastic Surgery · 25d

Cleared May 23, 1980

NDM DIATEMP ELECTROSURGICAL DIS. PAD

K801158 · GEI

General & Plastic Surgery · 9d

Cleared Apr 26, 1979

NDM PAPER TAPE ECG ELECTRODE

General Hospital · 35d

Cleared Nov 28, 1977

ELECTROSURGICAL GROUNDING PAD

K772160 · JOS

General & Plastic Surgery · 12d

Ndm Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Ndm Corp.

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