Medical Device Manufacturer · US , Mchenry , IL

Technicare Corp. - FDA 510(k) Cleared Devices

32 submissions · 32 cleared · Since 1980

Recent clearances: TECHNICARE 720 HPS CT SCANNER, SATURN NUCLEAR MEDICINE COMPUTER SYSTEM, AUTO DII MULTI FREQUENCY

Total

Cleared

Denied

Technicare Corp. has 32 FDA 510(k) cleared radiology devices. Based in Mchenry, US.

Historical record: 32 cleared submissions from 1980 to 1985.

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

Technicare 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 - Technicare Corp.

32 devices

1-12 of 32

Cleared Nov 15, 1985

TECHNICARE 720 HPS CT SCANNER

K854340 · JAK

Radiology · 18d

Cleared Jul 18, 1985

SATURN NUCLEAR MEDICINE COMPUTER SYSTEM

K852089 · IYX

Radiology · 66d

Cleared Feb 13, 1985

AUTO DII MULTI FREQUENCY

K844293 · IYN

Radiology · 100d

Cleared Jan 23, 1985

ULTRASONIC SCANNER CALIBRATION & TEST PHANTOMS

K844247 · GXX

Neurology · 83d

Cleared Dec 17, 1984

NUCLEAR 700 MEDICINE MECHANICAL POSIT-

K843716 · IYX

Radiology · 84d

Cleared Nov 29, 1984

AUTOFOCUS DUAL ELEMENT PROBE

K842777 · IYO

Radiology · 136d

Cleared Aug 17, 1984

TECHNICARE 248 SL & 260SL

TECHNICARE MODEL 1047

Technicare Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Technicare Corp.

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