Stellaris Elite vision enhancement system

FDA 510(k) K170052 · Bausch+Lomb

Substantially Equivalent

510(k) numberK170052

Submission

Device name
Stellaris Elite vision enhancement system
Applicant
Bausch+Lomb
St. Louis, MO, US
Received
January 5, 2017
Decision date
April 19, 2017
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HQC – Unit, Phacofragmentation
Device class
Class II (moderate risk)
Regulation
21 CFR 886.4670
Specialty
Ophthalmic

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Questions and answers

When was Stellaris Elite vision enhancement system cleared by the FDA?

Stellaris Elite vision enhancement system (K170052) received a 510(k) decision of Substantially Equivalent on April 19, 2017, 104 days after the submission was received.

What is the product code of K170052?

The FDA product code is HQC – Unit, Phacofragmentation, a Class II (moderate risk) device regulated under 21 CFR 886.4670.