LIQUID CHROMATO. COLUMNS
K-Number: K880724 · 1988-05-27
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Device Summary
Frequently Asked Questions
What is the LIQUID CHROMATO. COLUMNS?
LIQUID CHROMATO. COLUMNS is a medical device that received FDA 510(k) clearance on 1988-05-27. The listed applicant is Supelco, Inc.. The 510(k) number is K880724.
When did LIQUID CHROMATO. COLUMNS receive FDA 510(k) clearance?
LIQUID CHROMATO. COLUMNS received FDA 510(k) clearance on 1988-05-27, under 510(k) number K880724.
Who is the listed applicant for LIQUID CHROMATO. COLUMNS?
The FDA 510(k) record lists Supelco, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIQUID CHROMATO. COLUMNS?
The FDA product code for LIQUID CHROMATO. COLUMNS is DPM.
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 Supelco, 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: DPM)
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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