SLIT LAMP BO 900, BQ 900, BP900
K-Number: K100202 · 2010-03-19
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Device Summary
Frequently Asked Questions
What is the SLIT LAMP BO 900, BQ 900, BP900?
SLIT LAMP BO 900, BQ 900, BP900 is a medical device that received FDA 510(k) clearance on 2010-03-19. The listed applicant is Haag-Streit AG. The 510(k) number is K100202.
When did SLIT LAMP BO 900, BQ 900, BP900 receive FDA 510(k) clearance?
SLIT LAMP BO 900, BQ 900, BP900 received FDA 510(k) clearance on 2010-03-19, under 510(k) number K100202.
Who is the listed applicant for SLIT LAMP BO 900, BQ 900, BP900?
The FDA 510(k) record lists Haag-Streit AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SLIT LAMP BO 900, BQ 900, BP900?
The FDA product code for SLIT LAMP BO 900, BQ 900, BP900 is HJO.
Other records listing Haag-Streit AG 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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