Atlas FDA

ADVANCE DIAGNOSTICS DISPOSABLE EYECUP

FDA 510(k) clearance K881369 · decided 1988-05-13

Clearance details

K-number
K881369
Device name
ADVANCE DIAGNOSTICS DISPOSABLE EYECUP
Applicant
Advantage Diagnostics Corp.
Decision
Substantially Equivalent
Date received
1988-04-01
Decision date
1988-05-13
Days to decision
42 days
Clearance type
Traditional
Product code
LXQ
Device class
U
Medical specialty
Unknown
Advisory committee
Unknown
Location
Tucson, AZ, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Dynarex Eye Cups (K151575)Dynarex Corporation2015-09-01
FLENTS PLASTIC EYE WASH CUP (K140409)Apothecary Products, Inc.2014-07-09
EYE CUP, STERILE 1 AND NON STERILE (K051414)Tollot Pty.Ltd.(Aaxis Pacific)2005-06-16
VISTA EYESHOWER (K971134)John Branch1997-11-04

Recalls involving this device

No recalls on record reference this clearance.