Atlas FDA

FLUORESCENCE ILLUMINATOR ACCESSORY

FDA 510(k) clearance K770652 · decided 1977-07-06

Clearance details

K-number
K770652
Device name
FLUORESCENCE ILLUMINATOR ACCESSORY
Applicant
Bausch & Lomb, Inc.
Decision
Substantially Equivalent
Date received
1977-04-06
Decision date
1977-07-06
Days to decision
91 days
Clearance type
Traditional
Product code
IBK
Device class
1
Regulation number
864.3600
Medical specialty
Pathology
Advisory committee
Pathology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
Bausch & Lomb SofLens® (polymacon) Contact Lenses (N16895/S107)Bausch & Lomb, Inc.2025-10-24
Akreos Posterior Chamber Intraocular Lens (P060022/S037)Bausch & Lomb, Inc.2025-09-30
enVista Envy™ hydrophobic acrylic intraocular lens (IOL), enVista Envy™ toric hydrophobic acrylic intraocular lens (IOL) (P240005/S003)Bausch & Lomb, Inc.2025-07-30
Akreos Posterior Chamber Intraocular Lens (IOL) (P060022/S036)Bausch & Lomb, Inc.2025-07-22
Akreos Posterior Chamber Intraocular Lens (IOL) (P060022/S035)Bausch & Lomb, Inc.2025-07-09
enVista® Hydrophobic Acrylic Intraocular Lens (IOL) (P910056/S060)Bausch & Lomb, Inc.2025-06-18
enVista hydrophobic acrylic intraocular lens (IOL), enVista toric hydrophobic acrylic intraocular lens (IOL), enVista As (P910056/S059)Bausch & Lomb, Inc.2025-05-30
enVista Envy™ hydrophobic acrylic intraocular lens (IOL), enVista Envy™ toric hydrophobic acrylic intraocular lens (IOL) (P240005/S004)Bausch & Lomb, Inc.2025-05-30