510(k) K011069

AQUASENS FLUID MONITORING SYSTEM by Davol Inc., Sub. C. R. Bard, Inc. — Product Code HIG

K011069 is an FDA 510(k) premarket notification submitted by Davol Inc., Sub. C. R. Bard, Inc. for the device "AQUASENS FLUID MONITORING SYSTEM". The FDA issued a decision of Substantially Equivalent on August 16, 2001. The device falls under product code HIG (Insufflator, Hysteroscopic), a Class II device regulated under 21 CFR 884.1700. Davol Inc., Sub. C. R. Bard, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 16, 2001
Date Received
April 9, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
Yes

Device Classification

Device Name
Insufflator, Hysteroscopic
Device Class
Class II
Regulation Number
884.1700
Review Panel
OB
Submission Type