510(k) K770652
- Device
- FLUORESCENCE ILLUMINATOR ACCESSORY
- Applicant
- Bausch & Lomb, Inc.
- 510(k) number
- K770652
- Product code
- IBK
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-07-06
- Date received
- 1977-04-06
- Regulation
- 864.3600
- Classification name
- Microscope, Fluorescence/U.V.
- Medical specialty
- Pathology
- Review panel
- Pathology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- N
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3006610913
- 3015505238
- 3007123908
- 1320925
- 3021959405
- 3016418391
- 3007361513
- 3026040791
- 3008564898
- 8010666
- 3001111904
- 3021720733
- 1067123
- 9680625
- 3010399828
- 2435594
- 3005273623
- 2013736
- 3016621374
- 3021967177
- 3015376545
- 1217454
- 3010420046
- 3021744379
- 3003268355
- 3003893952
- 3026753391
- 3004545210
- 9613910
- 2916205
- 3007118747
Source Documents#
510(k) summary PDF not indicated by FDA