Medical Device Manufacturer · US , Walker , MI

Zeiss Humphrey System - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1979

Total

Cleared

Denied

Zeiss Humphrey System has 9 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 9 cleared submissions from 1979 to 1994. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Zeiss Humphrey System Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Zeiss Humphrey System

9 devices

1-9 of 9

Cleared Jul 01, 1994

ZEISS OPMILAS 144 SURGICAL LASERS

K942439 · GEX

General & Plastic Surgery · 112d

Cleared Nov 08, 1993

DIGITAL OPHTHALMIC ULTRASOUND BIOMICROSCOPE

K923211 · IYO

Radiology · 495d

Cleared Dec 10, 1992

OPHTHALMIC A/B SCAN SYSTEM, MODEL 835 -- MODIFIED

K923348 · ITX

Radiology · 196d

Cleared Sep 18, 1985

HUMPHREY FIELD ANALYZER MODEL 630

K852639 · HPT

Ophthalmic · 90d

Cleared Aug 12, 1985

HUMPHREY IMAGE ANALYZER MODEL 110

K852638 · HKI

Ophthalmic · 53d

Cleared Jul 28, 1982

THE HUMPHREY FIELD ANALYZER MODEL 610

AUTOKERATOMETER, INSTRUMENT

K781994 · HLQ

Ophthalmic · 75d

Cleared Jan 26, 1979

INSTRUMENTS, OVERREFRACTION SYSTEM

K782096 · HLM

Ophthalmic · 39d

Zeiss Humphrey System - FDA 510(k) Cleared Devices

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