Dorc Lightweight Binocular Ophthalmoscop

FDA 510(k) K830215 · Jedmed Instrument Co.

Substantially Equivalent

510(k) numberK830215

Submission

Device name
Dorc Lightweight Binocular Ophthalmoscop
Applicant
Jedmed Instrument Co.
Walker, MI, US
Received
January 24, 1983
Decision date
March 9, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HLJ – Ophthalmoscope, Battery-Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 886.1570
Specialty
Ophthalmic

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Questions and answers

When was Dorc Lightweight Binocular Ophthalmoscop cleared by the FDA?

Dorc Lightweight Binocular Ophthalmoscop (K830215) received a 510(k) decision of Substantially Equivalent on March 9, 1983, 44 days after the submission was received.

What is the product code of K830215?

The FDA product code is HLJ – Ophthalmoscope, Battery-Powered, a Class II (moderate risk) device regulated under 21 CFR 886.1570.