Medical Device Manufacturer · US , Richmond , VA

Pari Holding Co. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1994

Recent clearances: PRONEB ULTRA MODEL NUMBER 85B0100, RC CORNET, MODEL #44F50, PARI PEP THERAPY SYSTEM

View 8 510(k) Devices ↓

Total

Cleared

Denied

Pari Holding Co. has 8 FDA 510(k) cleared medical devices. Based in Richmond, US.

Historical record: 8 cleared submissions from 1994 to 2001. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Pari Holding Co. Filter by specialty or product code using the sidebar.

Pari Holding Co. is one of 20391 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Pari Holding Co.

8 devices

1-8 of 8

Cleared Mar 13, 2001

PRONEB ULTRA MODEL NUMBER 85B0100

K002862 · BTI

Anesthesiology · 181d

Cleared Jun 04, 1999

RC CORNET, MODEL #44F50

K983308 · BWF

Anesthesiology · 256d

Cleared Aug 05, 1997

PARI PEP THERAPY SYSTEM

K972042 · BWF

Anesthesiology · 64d

Cleared Dec 10, 1996

LC STAR REUSABLE NEBULIZER 22F50 AND LC STAR DISPOSABLE NEBULIZER 22F70

K963924 · CAF

Anesthesiology · 71d

Cleared Aug 21, 1996

PRONEB TURBO COMPRESSOR MODEL 38V0200

K962072 · CAF

Anesthesiology · 85d

Cleared May 17, 1996

WALKHALER PORTABLE COMPRESSOR MODEL 45F70

K960675 · CAF

Anesthesiology · 87d

Cleared Mar 17, 1995

PARI-MASTER MODIFICATION

K935540 · CAF

Anesthesiology · 486d

Pari Holding Co. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Pari Holding Co.

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