Medical Device Manufacturer · US , Mchenry , IL

Science Development Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1983

Total

Cleared

Denied

Science Development Corp. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1983 to 1984. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Science Development Corp.

9 devices

1-9 of 9

Cleared Oct 24, 1984

SDC SILICONE SUMP DRAIN

K843617 · GBX

General & Plastic Surgery · 40d

Cleared Aug 10, 1984

SDC SILICONE FORCEP SHODS PRODUCT

K842491

General & Plastic Surgery · 45d

Cleared Jan 27, 1984

SDC VASCULAR TIES

K833355 · KDC

General & Plastic Surgery · 121d

Cleared Oct 31, 1983

SCD SKIN TEMP. SENSORS #3400 ETC

K832090 · FLL

General Hospital · 125d

Cleared Sep 12, 1983

QT-100 ELECTRONIC TEMP. MONITOR

K832391 · FLL

General Hospital · 55d

Cleared Sep 12, 1983

SDC ORAL-RECTAL TEMP. PROBE

K832392 · FLL

General Hospital · 55d

Cleared Apr 06, 1983

ESOPHAGEAL PROBE W/TEMP. INDICATOR

K830353 · FLL

General Hospital · 62d

Cleared Mar 11, 1983

ESOPHAGEAL STETHOSCOPE

K830329 · BZW

Anesthesiology · 38d

Cleared Feb 23, 1983

SDC RECTAL TEMP. PROBE PRODUCT #1020

K830039 · FLL

General Hospital · 47d

Science Development Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Science Development Corp.

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