Atlas FDA

YELLOW 560 Fluorescence Module

FDA 510(k) clearance K162991 · decided 2017-07-24

Clearance details

K-number
K162991
Device name
YELLOW 560 Fluorescence Module
Applicant
Carl Zeiss Meditec, AG
Decision
Unknown
Date received
2016-10-27
Decision date
2017-07-24
Days to decision
270 days
Clearance type
Traditional
Product code
IZI
Device class
2
Regulation number
892.1600
Medical specialty
Radiology
Advisory committee
Radiology
Location
Jena, DE
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
VISULAS 690 PLUS LASER & VISULINK PDT/U ADAPTER (P990048/S003)Carl Zeiss Meditec, AG2008-10-31
VISULAS 690S AND VISULINK PDT/U ADAPTER (P990048/S001)Carl Zeiss Meditec, AG2001-09-27
VISULAS 690S LASER AND VISULINK PDT ADAPTER (P990048/S002)Carl Zeiss Meditec, AG2001-07-03
ZEISS VISULAS 690 LASER AND VISULINK PDT ADAPTER (P990048)Carl Zeiss Meditec, AG2000-04-12
MENTOR POSTERIOR CHAMBER INTRAOCULAR UV ABSORBING PMMA LENSES (P830056/S079)Carl Zeiss Meditec, AG1999-05-11
POSTERIOR CHAMBER INTRAOCULAR LENSES (TIER A SUBMISSION) (P830056/S078)Carl Zeiss Meditec, AG1998-01-29
POSTERIOR CHAMBER INTROCULAR LENSES (P830056/S077)Carl Zeiss Meditec, AG1996-08-01
POSTERIOR CHAMBER INTROCULAR LENSES (P830056/S075)Carl Zeiss Meditec, AG1996-04-02