INVIGRA— 510(k) K020223

Substantially Equivalent

Indus Medicare , Ltd.

FDA 510(k) clearance K020223 for INVIGRA, Substantially Equivalent on 2002-03-04. Applicant: Indus Medicare , Ltd.. Device class: 2.

Clearance details

Applicant: Indus Medicare , Ltd.
Product code: Code HIS
Device class: Class 2
Regulation: 21 CFR 884.5300
Advisory panel: Obstetrics/Gynecology
Date received: 2002-01-22
Decision date: 2002-03-04
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Hyderabad Andhra Pradesh, IN

Download summary PDF View on FDA.gov ↗

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More clearances from Indus Medicare , Ltd.

K022614 — INVIGRA2003-04-08
K000038 — INVIGRA MALE LATEX CONDOM GREEN COLORED AND MINT FLAVORED2000-03-21
K000039 — INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED2000-03-21
K000040 — INVIGRA MALE LATEX CONDOM BLUE COLORED AND VANILLA FLAVORED2000-03-21
K993693 — INVIGRA1999-12-29

Data sourced from openFDA. This site is unofficial and independent of the FDA.