510(k) K883806

ROCKET INTRAUTERINE SOUND by A & A Medical, Inc. — Product Code HHM

K883806 is an FDA 510(k) premarket notification submitted by A & A Medical, Inc. for the device "ROCKET INTRAUTERINE SOUND". The FDA issued a decision of Substantially Equivalent on October 31, 1988. The device falls under product code HHM (Sound, Uterine), a Class I device regulated under 21 CFR 884.4530. A & A Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 31, 1988
Date Received
September 7, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Sound, Uterine
Device Class
Class I
Regulation Number
884.4530
Review Panel
OB
Submission Type