Medical Device Manufacturer · US , Lebanon , NJ

Interpro Intl., Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1987

Total

Cleared

Denied

Interpro Intl., Inc. has 11 FDA 510(k) cleared general hospital devices. Based in Lebanon, US.

Historical record: 11 cleared submissions from 1987 to 1989.

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

Interpro Intl., Inc. 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 - Interpro Intl., Inc.

11 devices

1-11 of 11

Cleared Jul 31, 1989

VINYL EXAMINATION GLOVES (MFG. SALZGITTER MOREX)

K890968 · LYZ

General Hospital · 154d

Cleared Jul 14, 1989

LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL)

K890891 · LYY

General Hospital · 142d

Cleared Jul 14, 1989

PATIENT EXAMINATION GLOVES (LATEX)

K891642 · LYY

General Hospital · 119d

Cleared May 31, 1989

PATIENT EXAMINATION GLOVES (LATEX)

K891438 · LYY

General Hospital · 77d

Cleared May 31, 1989

PATIENT EXAMINATION GLOVES (LATEX)

K891440 · LYY

General Hospital · 77d

Cleared Aug 05, 1988

SURGEONS GLOVES

K881374 · KGO

General Hospital · 126d

Cleared Dec 14, 1987

GUAZE SPONGES

K874067 · EFQ

General & Plastic Surgery · 70d

Cleared Dec 10, 1987

INTERPRO INT'L, INC. ISOLATION GOWN

K874766 · FYC

General Hospital · 21d

Cleared Nov 04, 1987

SHOE COVERS

K874064 · FXP

General Hospital · 30d

Cleared Nov 04, 1987

LAPAROTOMY SPONGES

K874065 · EFQ

General & Plastic Surgery · 30d

Cleared Nov 04, 1987

SURGICAL CAPS

K874066 · FYF

General & Plastic Surgery · 30d

Interpro Intl., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Interpro Intl., Inc.

Filters