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FDA 510(k)

CAPILLARY COLUMNS FOR GAS CHROMATOGRAPHY

K-Number: K862542 · 1986-08-04

ApplicantSupelco, Inc.
Decision Date1986-08-04
Product CodeDII
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CAPILLARY COLUMNS FOR GAS CHROMATOGRAPHY is the device name listed in this FDA 510(k) record. The listed applicant is Supelco, Inc.. It received FDA 510(k) clearance on 1986-08-04 under 510(k) number K862542. The device is classified under product code DII. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPILLARY COLUMNS FOR GAS CHROMATOGRAPHY?

CAPILLARY COLUMNS FOR GAS CHROMATOGRAPHY is a medical device that received FDA 510(k) clearance on 1986-08-04. The listed applicant is Supelco, Inc.. The 510(k) number is K862542.

When did CAPILLARY COLUMNS FOR GAS CHROMATOGRAPHY receive FDA 510(k) clearance?

CAPILLARY COLUMNS FOR GAS CHROMATOGRAPHY received FDA 510(k) clearance on 1986-08-04, under 510(k) number K862542.

Who is the listed applicant for CAPILLARY COLUMNS FOR GAS CHROMATOGRAPHY?

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 COLUMNS FOR GAS CHROMATOGRAPHY?

The FDA product code for CAPILLARY COLUMNS FOR GAS CHROMATOGRAPHY 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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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