ZEISS 40 SL/P PHOTO SLIT LAMP
K-Number: K874160 · 1988-01-27
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Device Summary
Frequently Asked Questions
What is the ZEISS 40 SL/P PHOTO SLIT LAMP?
ZEISS 40 SL/P PHOTO SLIT LAMP is a medical device that received FDA 510(k) clearance on 1988-01-27. The listed applicant is Carl Zeiss, Inc.. The 510(k) number is K874160.
When did ZEISS 40 SL/P PHOTO SLIT LAMP receive FDA 510(k) clearance?
ZEISS 40 SL/P PHOTO SLIT LAMP received FDA 510(k) clearance on 1988-01-27, under 510(k) number K874160.
Who is the listed applicant for ZEISS 40 SL/P PHOTO SLIT LAMP?
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 40 SL/P PHOTO SLIT LAMP?
The FDA product code for ZEISS 40 SL/P PHOTO SLIT LAMP is HJO.
Related Clinical Trials
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.
Other records listing Carl Zeiss, Inc. as applicant
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.
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.
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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