BURTON HAND HELD SLIT LAMP - MODEL SL750
K-Number: K924770 · 1993-01-27
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Device Summary
Frequently Asked Questions
What is the BURTON HAND HELD SLIT LAMP - MODEL SL750?
BURTON HAND HELD SLIT LAMP - MODEL SL750 is a medical device that received FDA 510(k) clearance on 1993-01-27. The listed applicant is R.H. Burton Co.. The 510(k) number is K924770.
When did BURTON HAND HELD SLIT LAMP - MODEL SL750 receive FDA 510(k) clearance?
BURTON HAND HELD SLIT LAMP - MODEL SL750 received FDA 510(k) clearance on 1993-01-27, under 510(k) number K924770.
Who is the listed applicant for BURTON HAND HELD SLIT LAMP - MODEL SL750?
The FDA 510(k) record lists R.H. Burton Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BURTON HAND HELD SLIT LAMP - MODEL SL750?
The FDA product code for BURTON HAND HELD SLIT LAMP - MODEL SL750 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 R.H. Burton Co. 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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