510(k) K020223
K020223 is an FDA 510(k) premarket notification submitted by Indus Medicare , Ltd. for the device "INVIGRA". The FDA issued a decision of Substantially Equivalent on March 4, 2002. The device falls under product code HIS (Condom), a Class II device regulated under 21 CFR 884.5300. Indus Medicare , Ltd. has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 4, 2002
- Date Received
- January 22, 2002
- Clearance Type
- Abbreviated
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Condom
- Device Class
- Class II
- Regulation Number
- 884.5300
- Review Panel
- OB
- Submission Type