510(k) K960630
- Device
- ANSPAHC SPEED REDUCER
- Applicant
- The Anspach Effort, Inc.
- 510(k) number
- K960630
- Product code
- HBB
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1996-11-19
- Date received
- 1996-02-09
- Regulation
- 882.4370
- Classification name
- Motor, Drill, Pneumatic
- Medical specialty
- Neurology
- Review panel
- Neurology
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Statement
- Third party reviewed
- No
Applicant Contact#
- Contact
- WILLIAM E ANSPACH
- Address
- 4500 Riverside Dr. Palm Beach Gardens FL US 33410 33410
FDA Registration Numbers#
- 3040335671
- 3036756245
- 3015967359
- 3003120897
- 3004464325
- 3010173425
- 9616696
- 3017210488
- 3014479313
- 1058584
- 9610612
- 3008812560
- 2916714
- 3002807310
- 3001239363
- 1045834
- 1834331
- 8030965
- 3000270450
- 1030489
- 1000200989
- 3009417901
- 3005382983
- 2647346
- 1625507
- 3010155648
- 2648623
- 3033509898
- 3021632375
- 3007031059
- 3015453963
- 3025603301
- 3007997036
- 3004598644
- 3018094310
- 3003595343
- 1649518
- 1723170
- 1828288
- 1048735
- 3016172274
- 1045254
- 3008868758
- 1061124
- 1017294
Source Documents#
510(k) summary PDF not indicated by FDA
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