Medical Device Manufacturer · US , Mchenry , IL

Medi Nuclear Corp., Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1981

Total

Cleared

Denied

Medi Nuclear Corp., Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1981 to 2008. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Medi Nuclear Corp., Inc.

9 devices

1-9 of 9

Cleared Nov 26, 2008

HEALTHLINE MEDICATOR / REDINEB AEROSOL DRUG DELIVERY SYSTEM

K082541 · CAF

Anesthesiology · 85d

Cleared Jul 25, 2008

HEALTHLINE REDI-NEB MEDICATION NEBULIZER, MODEL RN-510

K080969 · CAF

Anesthesiology · 112d

Cleared Jun 30, 2008

NEB-90 LARGE VOLUME MEDICATION NEBULIZER

K080657 · CAF

Anesthesiology · 115d

Cleared Jul 16, 1992

NEBULIZER (DIRECT PATIENT INTERFACE)

K915075 · CAF

Anesthesiology · 251d

Cleared Oct 20, 1987

AERO-VENT AEROSOL UNIT

K865107 · IYT

Radiology · 293d

Cleared Jan 15, 1987

SAFE-T-SHIELD MOUTHPIECE

K865093 · BYP

Anesthesiology · 16d

Cleared Nov 04, 1986

MODEL XE-103 XENON/MASTER II

K863996 · IYT

Radiology · 21d

Cleared Jan 22, 1982

RADIONUCLIDE DOSE CALIBRATOR

K813379 · KPT

Radiology · 52d

Cleared Apr 14, 1981

MEDI/NUCLEAR #XE-102 XENON/MASTER

K810819 · IYT

Radiology · 21d

Medi Nuclear Corp., Inc. - FDA 510(k) Cleared Devices

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