Visitec Ophthalmic Aspiration Unit Model 100

FDA 510(k) K853961 · Visitec Co.

Substantially Equivalent

510(k) numberK853961

Submission

Device name
Visitec Ophthalmic Aspiration Unit Model 100
Applicant
Visitec Co.
Sarasota, FL, US
Received
September 25, 1985
Decision date
December 13, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HQE – Instrument, Vitreous Aspiration And Cutting, Ac-Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 886.4150
Specialty
Ophthalmic

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Questions and answers

When was Visitec Ophthalmic Aspiration Unit Model 100 cleared by the FDA?

Visitec Ophthalmic Aspiration Unit Model 100 (K853961) received a 510(k) decision of Substantially Equivalent on December 13, 1985, 79 days after the submission was received.

What is the product code of K853961?

The FDA product code is HQE – Instrument, Vitreous Aspiration And Cutting, Ac-Powered, a Class II (moderate risk) device regulated under 21 CFR 886.4150.