HOSKINS NYLON SUTURE LASER LENS

Lens, Contact, Polymethylmethacrylate, Diagnostic

OCULAR INSTRUMENTS, INC.

The following data is part of a premarket notification filed by Ocular Instruments, Inc. with the FDA for Hoskins Nylon Suture Laser Lens.

Pre-market Notification Details

Device IDK862728
510k NumberK862728
Device Name:HOSKINS NYLON SUTURE LASER LENS
ClassificationLens, Contact, Polymethylmethacrylate, Diagnostic
Applicant OCULAR INSTRUMENTS, INC. 12100 NORTHUP WAY SUITE D Bellevue,  WA  98005
ContactTamsin J Erickson
CorrespondentTamsin J Erickson
OCULAR INSTRUMENTS, INC. 12100 NORTHUP WAY SUITE D Bellevue,  WA  98005
Product CodeHJK  
CFR Regulation Number886.1385 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1986-07-18
Decision Date1986-08-21

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00630238106511 K862728 000
00630238100007 K862728 000
00630238007054 K862728 000

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