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Interpro Intl., Inc.

Lebanon, NJ, US

Interpro Intl., Inc. appears in FDA device records in Lebanon, NJ. FDA records list 11 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
11
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 11 510(k) clearances for Interpro Intl., Inc. between 1987 and 1989. The busiest year on record is 1987, with 5. The most recent is 1989, with 5.

Clearances by year, as a table
510(k) clearance decisions for Interpro Intl., Inc., by decision year
YearClearances
19875
19881
19895
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K890968VINYL EXAMINATION GLOVES (MFG. SALZGITTER MOREX)LYZSubstantially Equivalent
K891642PATIENT EXAMINATION GLOVES (LATEX)LYYSubstantially Equivalent
K890891LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL)LYYSubstantially Equivalent
K891440PATIENT EXAMINATION GLOVES (LATEX)LYYSubstantially Equivalent
K891438PATIENT EXAMINATION GLOVES (LATEX)LYYSubstantially Equivalent
K881374SURGEONS GLOVESKGOSubstantially Equivalent
K874067GUAZE SPONGESEFQSubstantially Equivalent
K874766INTERPRO INT'L, INC. ISOLATION GOWNFYCSubstantially Equivalent
K874066SURGICAL CAPSFYFSubstantially Equivalent
K874065LAPAROTOMY SPONGESEFQSubstantially Equivalent
K874064SHOE COVERSFXPSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain