Medical Device Manufacturer · US , Mchenry , IL

Lectec Corp. - FDA 510(k) Cleared Devices

27 submissions · 26 cleared · Since 1977

Total

Cleared

Denied

Lectec Corp. has 26 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 26 cleared submissions from 1977 to 1996. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Lectec Corp.

27 devices

1-12 of 27

ISOPORE(TM) TAPE, MODIFICATION

K925384 · KGX

General & Plastic Surgery · 177d

Cardiovascular · 216d

Cleared Sep 11, 1992

ISOPORE TAPE

K922959 · KGX

General & Plastic Surgery · 85d

Cardiovascular · 121d

MACROPORE MEDICAL/SURGICAL PAPER TAPE

K884108 · KGX

General & Plastic Surgery · 42d

Cleared Jul 20, 1988

SYNCOR (R) MODEL S-801 ECG ELECTRODE

K882216 · DRX

Cardiovascular · 55d

Cleared Jun 16, 1988

SPARE MS 700 TENS ELECTRODE

K881871 · GXY

Neurology · 44d

Cleared Jun 16, 1988

TENS ELECTRODE MODEL 238P

K881872 · GXY

Neurology · 44d

Lectec Corp. - FDA 510(k) Cleared Devices

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