APPASAMY SLIT LAMP, A1A-11 AND A1A-12 SERIES
K-Number: K082031 · 2008-07-31
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Device Summary
Frequently Asked Questions
What is the APPASAMY SLIT LAMP, A1A-11 AND A1A-12 SERIES?
APPASAMY SLIT LAMP, A1A-11 AND A1A-12 SERIES is a medical device that received FDA 510(k) clearance on 2008-07-31. The listed applicant is Appasamy Associates. The 510(k) number is K082031.
When did APPASAMY SLIT LAMP, A1A-11 AND A1A-12 SERIES receive FDA 510(k) clearance?
APPASAMY SLIT LAMP, A1A-11 AND A1A-12 SERIES received FDA 510(k) clearance on 2008-07-31, under 510(k) number K082031.
Who is the listed applicant for APPASAMY SLIT LAMP, A1A-11 AND A1A-12 SERIES?
The FDA 510(k) record lists Appasamy Associates as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for APPASAMY SLIT LAMP, A1A-11 AND A1A-12 SERIES?
The FDA product code for APPASAMY SLIT LAMP, A1A-11 AND A1A-12 SERIES 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 Appasamy Associates 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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