510(k) K931822
- Device
- CARAPACE PELVIC EXAM TRAYS
- Applicant
- Carapace, Inc.
- 510(k) number
- K931822
- Product code
- MLT
- Decision
- Unknown (SESK)
- Decision date
- 1994-03-07
- Date received
- 1993-04-08
- Regulation
- 884.4530
- Classification name
- Pelvic Exam Kit
- Medical specialty
- Obstetrics/Gynecology
- Review panel
- Obstetrics/Gynecology
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Statement
- Third party reviewed
- N
Applicant Contact#
- Contact
- JERRY W MEYERS
- Address
- 2701 W Concord St. Broken Arrow OK US 74012 74012
FDA Registration Numbers#
- 9616088
- 2433012
- 1061124
- 1047429
- 3004122598
- 3005012805
- 1423537
- 3035642068
- 3009888344
- 3015173212
- 1824619
- 1423395
- 1928237
- 3007329020
- 1643817
- 1054241
- 1043214
- 3004111573
- 3004519921
- 1055236
- 1030451
- 1422634
- 2029015
Source Documents#
510(k) summary PDF not indicated by FDA