LIQUID CHROMATOGRAPHY (HPLC) COLUMNS
K-Number: K813575 · 1982-01-18
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Device Summary
Frequently Asked Questions
What is the LIQUID CHROMATOGRAPHY (HPLC) COLUMNS?
LIQUID CHROMATOGRAPHY (HPLC) COLUMNS is a medical device that received FDA 510(k) clearance on 1982-01-18. The listed applicant is Supelco, Inc.. The 510(k) number is K813575.
When did LIQUID CHROMATOGRAPHY (HPLC) COLUMNS receive FDA 510(k) clearance?
LIQUID CHROMATOGRAPHY (HPLC) COLUMNS received FDA 510(k) clearance on 1982-01-18, under 510(k) number K813575.
Who is the listed applicant for LIQUID CHROMATOGRAPHY (HPLC) 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 CHROMATOGRAPHY (HPLC) COLUMNS?
The FDA product code for LIQUID CHROMATOGRAPHY (HPLC) 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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