INVIGRA— 510(k) K991374

Substantially Equivalent

Indus Medicare , Ltd.

FDA 510(k) clearance K991374 for INVIGRA, Substantially Equivalent on 1999-06-15. 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: 1999-04-21
Decision date: 1999-06-15
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
K020223 — INVIGRA2002-03-04
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

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