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FDA 510(k)

ZEISS 20 SL SLIT-LAMP & MECHANICAL MICROMANIPULATR

K-Number: K925641 · 1993-09-09

ApplicantCarl Zeiss, Inc.
Decision Date1993-09-09
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ZEISS 20 SL SLIT-LAMP & MECHANICAL MICROMANIPULATR is the device name listed in this FDA 510(k) record. The listed applicant is Carl Zeiss, Inc.. It received FDA 510(k) clearance on 1993-09-09 under 510(k) number K925641. The device is classified under product code HJO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZEISS 20 SL SLIT-LAMP & MECHANICAL MICROMANIPULATR?

ZEISS 20 SL SLIT-LAMP & MECHANICAL MICROMANIPULATR is a medical device that received FDA 510(k) clearance on 1993-09-09. The listed applicant is Carl Zeiss, Inc.. The 510(k) number is K925641.

When did ZEISS 20 SL SLIT-LAMP & MECHANICAL MICROMANIPULATR receive FDA 510(k) clearance?

ZEISS 20 SL SLIT-LAMP & MECHANICAL MICROMANIPULATR received FDA 510(k) clearance on 1993-09-09, under 510(k) number K925641.

Who is the listed applicant for ZEISS 20 SL SLIT-LAMP & MECHANICAL MICROMANIPULATR?

The FDA 510(k) record lists Carl Zeiss, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ZEISS 20 SL SLIT-LAMP & MECHANICAL MICROMANIPULATR?

The FDA product code for ZEISS 20 SL SLIT-LAMP & MECHANICAL MICROMANIPULATR is HJO.

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Other records listing Carl Zeiss, Inc. as applicant

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Related Devices (Code: HJO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262637SLIT LAMP SL-D4 (Type: LED)Topcon CorporationK253834VISUREF 600Carl Zeiss Vision GmbHK231760HP-OCT (HP-OCT)Cylite Pty. , Ltd.K222372Kowa SL-19Kowa Company , Ltd.K193188MiiS Horus Eye Anterior CameraMedimaging Integrated Solution, Inc (Miis)K182306Sunkingdom Slit LampChongqing Sunkingdom Medical Instrument Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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