CAPILLARY GAS CHROMATOGRAPHIC COLUMNS
K-Number: K841712 · 1984-05-21
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Device Summary
Frequently Asked Questions
What is the CAPILLARY GAS CHROMATOGRAPHIC COLUMNS?
CAPILLARY GAS CHROMATOGRAPHIC COLUMNS is a medical device that received FDA 510(k) clearance on 1984-05-21. The listed applicant is Supelco, Inc.. The 510(k) number is K841712.
When did CAPILLARY GAS CHROMATOGRAPHIC COLUMNS receive FDA 510(k) clearance?
CAPILLARY GAS CHROMATOGRAPHIC COLUMNS received FDA 510(k) clearance on 1984-05-21, under 510(k) number K841712.
Who is the listed applicant for CAPILLARY GAS CHROMATOGRAPHIC 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 CAPILLARY GAS CHROMATOGRAPHIC COLUMNS?
The FDA product code for CAPILLARY GAS CHROMATOGRAPHIC COLUMNS 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 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: 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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