510(k) K800956

DOUCH TRAY-DISPOSABLE VAGINAL TRAY W/BEN by The Healthcare Group Laboratories, Inc. — Product Code HED

K800956 is an FDA 510(k) premarket notification submitted by The Healthcare Group Laboratories, Inc. for the device "DOUCH TRAY-DISPOSABLE VAGINAL TRAY W/BEN". The FDA issued a decision of Substantially Equivalent on October 3, 1980. The device falls under product code HED (Douche Apparatus, Vaginal, Therapeutic), a Class I device regulated under 21 CFR 884.5900. The Healthcare Group Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 3, 1980
Date Received
April 23, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Douche Apparatus, Vaginal, Therapeutic
Device Class
Class I
Regulation Number
884.5900
Review Panel
OB
Submission Type