19091-XXXXX SER. OF GLASS CAPILLARY COL.
K-Number: K791893 · 1979-10-30
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Device Summary
Frequently Asked Questions
What is the 19091-XXXXX SER. OF GLASS CAPILLARY COL.?
19091-XXXXX SER. OF GLASS CAPILLARY COL. is a medical device that received FDA 510(k) clearance on 1979-10-30. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K791893.
When did 19091-XXXXX SER. OF GLASS CAPILLARY COL. receive FDA 510(k) clearance?
19091-XXXXX SER. OF GLASS CAPILLARY COL. received FDA 510(k) clearance on 1979-10-30, under 510(k) number K791893.
Who is the listed applicant for 19091-XXXXX SER. OF GLASS CAPILLARY COL.?
The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 19091-XXXXX SER. OF GLASS CAPILLARY COL.?
The FDA product code for 19091-XXXXX SER. OF GLASS CAPILLARY COL. is DII.
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 Hewlett-Packard 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: DII)
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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