Home / Device Classification / HEE

HEE — Set, Anesthesia, Paracervical Class II

FDA Device Classification

Classification Details

Product Code
HEE
Device Class
Class II
Regulation Number
884.5100
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K052365rocket medicalCERVINEEDLE DISPOSABLE CARTRIDGE SYRINGEOctober 17, 2005
K021224wallach surgical devicesENDOCERVICAL BLOCK NEEDLEJuly 12, 2002
K000117avid medicalAVID-NIT CERVICAL REGIONAL ANESTHESIA NEEDLEApril 13, 2000
K983897ri mosCERVICAL ANESTHESIA NEEDLE, CONTRACERVICAL ANESTHESIA NEEDLE, MODEL #'S 720209 3February 1, 1999
K980238gynexGYNEX EXTENDED REACH NEEDLEAugust 21, 1998
K973671a and a medicalENDOCERVICAL BLOCK NEEDLENovember 26, 1997
K954718ellman intlELLMAN NEEDLE EXTENDER/MEASURED DOSE SYRINGEFebruary 29, 1996
K910253coopersurgicalLEEP REDIKITApril 18, 1991
K910252coopersurgicalPOTOCKY NEDDLE (TM) DISPOSABLE INJECTION NEEDLEMarch 4, 1991