510(k) K883805

ROCKET SEX CRIME KIT by A & A Medical, Inc. — Product Code FMC

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