510(k) K883805
K883805 is an FDA 510(k) premarket notification submitted by A & A Medical, Inc. for the device "ROCKET SEX CRIME KIT". The FDA issued a decision of Substantially Equivalent on January 31, 1989. The device falls under product code FMC (Patient Examination Glove), a Class I device regulated under 21 CFR 880.6250. A & A Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 31, 1989
- Date Received
- September 7, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Patient Examination Glove
- Device Class
- Class I
- Regulation Number
- 880.6250
- Review Panel
- HO
- Submission Type