510(k) K223381
- Device
- iExaminer System with Panoptic Plus
- Applicant
- Welch Allyn, Inc.
- 510(k) number
- K223381
- Product code
- HKI
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2023-03-15
- Date received
- 2022-11-07
- Regulation
- 886.1120
- Classification name
- Camera, Ophthalmic, Ac-Powered
- Medical specialty
- Ophthalmic
- Review panel
- Ophthalmic
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- N
Related Records
Applicant Contact
- Contact
- Jeffrey E. Thompson
- Address
- (A Subsidiary Of Baxter Healthcare Corporation) 4341 State St. Rd. Skaneateles Falls NY US 13153 13153
FDA Registration Numbers
- 1319721
- 3005950902
- 3008396732
- 3003144120
- 2521877
- 1528142
- 3038614464
- 3012162565
- 3013403214
- 3016589969
- 3017175640
- 3010792309
- 3010363436
- 3010000450
- 9612197
- 2320749
- 2936921
- 3038790635
- 1316463
- 3008252121
- 1054713
- 3005755367
- 9614661
- 3009746052
- 3004443844
- 2080939
- 3010394097
- 2027009
- 3006087789
- 3011223751
- 3004441848
- 2242863
- 3004026651
- 3008729548
- 3005785090
- 3009173773
- 2918630
- 2020550
- 3006546174
- 3010069263
- 3002807715
- 3015316279
- 3003500271
- 3007237389
- 3009990264
- 3004848970
- 9616199
- 8010482
- 3007710608
- 3010202439
- 3015972897
- 3014606890
- 9617474
- 3003771740
- 8030392
- 3007913988
- 3008169506
- 1926681
- 3014342096
- 1000181430
- 1000391004
- 8020986
- 9615030
- 1222616
- 3012096560
- 3038356864
Source Documents
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