510(k) K884290
- Device
- Baxter Disposable Circumcision Tray
- Applicant
- BAXTER HEALTHCARE CORP.
- 510(k) number
- K884290
- Product code
- HFX
- Decision
- Unknown (SESD)
- Decision date
- 1988-12-08
- Date received
- 1988-10-12
- Regulation
- 884.4530
- Classification name
- Clamp, Circumcision
- Medical specialty
- Obstetrics/Gynecology
- Review panel
- Obstetrics/Gynecology
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- N
Related Records
Applicant Contact
- Contact
- MORIZIO, R.N.
- Address
- 7280 N. Caldwell Niles IL US 60648 60648
FDA Registration Numbers
- 9611112
- 3004111573
- 2916714
- 3008403546
- 3017907745
- 3015895045
- 3005595283
- 3006061749
- 9612030
- 1423507
- 1061124
- 3004519921
- 8010099
- 1422634
- 3005739654
- 3010041511
- 1720929
- 8040263
- 1921846
- 3035642068
- 3004598675
- 3027556548
- 3008338766
- 1018470
- 1030451
- 3004215117
- 1058584
- 3015173212
- 9710524
- 1722684
- 1720747
- 3005012805
- 3013358456
- 3002090132
- 3011137372
- 1123010
- 3012936366
- 1417592
- 3003644849
- 1423537
- 1928237
- 9616088
- 3011499367
- 3003322138
- 2431166
- 1924066
- 8040233
- 1824619
- 1836161
Source Documents
510(k) summary PDF not indicated by FDA
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