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FDA 510(k)

ZEISS 30 SL-L

K-Number: K862004 · 1986-06-17

ApplicantCarl Zeiss, Inc.
Decision Date1986-06-17
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ZEISS 30 SL-L 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 1986-06-17 under 510(k) number K862004. 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 30 SL-L?

ZEISS 30 SL-L is a medical device that received FDA 510(k) clearance on 1986-06-17. The listed applicant is Carl Zeiss, Inc.. The 510(k) number is K862004.

When did ZEISS 30 SL-L receive FDA 510(k) clearance?

ZEISS 30 SL-L received FDA 510(k) clearance on 1986-06-17, under 510(k) number K862004.

Who is the listed applicant for ZEISS 30 SL-L?

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 30 SL-L?

The FDA product code for ZEISS 30 SL-L 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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