Haag-Streit Slit Lamp 900

FDA 510(k) K792083 · Lumenis, Inc.

Substantially Equivalent

510(k) numberK792083

Submission

Device name
Haag-Streit Slit Lamp 900
Applicant
Lumenis, Inc.
Mchenry, IL, US
Received
October 16, 1979
Decision date
November 16, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HRM – Microscope, Operating & Accessories, Ac-Powered, Ophthalmic
Device class
Class I (low risk)
Regulation
21 CFR 878.4700
Specialty
General, Plastic Surgery

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K891001Microscope Knob Cover, Sterile, DisposableHRM · Traditional Prescott'S, Inc.04/11/1989SE
K854440Modified Clinical Widefield Specular Microscope 50HRM · Traditional Keeler Instruments, Inc.12/16/1985SE
K853855Xtal X-150 Operating MicroscopeHRM · Traditional Xtal Corp.10/15/1985SE
K852586Cromic Surgical Microscope Model MC-1HRM · Traditional Seltrex, Corp.07/30/1985SE
K852150Clinical Widefield Specular Micriscope 500HRM · Traditional Keeler Instruments, Inc.06/03/1985SE

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Questions and answers

When was Haag-Streit Slit Lamp 900 cleared by the FDA?

Haag-Streit Slit Lamp 900 (K792083) received a 510(k) decision of Substantially Equivalent on November 16, 1979, 31 days after the submission was received.

What is the product code of K792083?

The FDA product code is HRM – Microscope, Operating & Accessories, Ac-Powered, Ophthalmic, a Class I (low risk) device regulated under 21 CFR 878.4700.