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FDA 510(k)

GAS-CHROMATOGRAPHIC PACKING

K-Number: K801833 · 1980-08-27

ApplicantSupelco, Inc.
Decision Date1980-08-27
Product CodeDJA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GAS-CHROMATOGRAPHIC PACKING is the device name listed in this FDA 510(k) record. The listed applicant is Supelco, Inc.. It received FDA 510(k) clearance on 1980-08-27 under 510(k) number K801833. The device is classified under product code DJA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GAS-CHROMATOGRAPHIC PACKING?

GAS-CHROMATOGRAPHIC PACKING is a medical device that received FDA 510(k) clearance on 1980-08-27. The listed applicant is Supelco, Inc.. The 510(k) number is K801833.

When did GAS-CHROMATOGRAPHIC PACKING receive FDA 510(k) clearance?

GAS-CHROMATOGRAPHIC PACKING received FDA 510(k) clearance on 1980-08-27, under 510(k) number K801833.

Who is the listed applicant for GAS-CHROMATOGRAPHIC PACKING?

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 GAS-CHROMATOGRAPHIC PACKING?

The FDA product code for GAS-CHROMATOGRAPHIC PACKING is DJA.

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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.

K894141LIQUID CHROMATOGRAPHY COLUMNSK884403LIQUID CHROMATOGRAPHY COLUMNS SOLID PHASE EX. TUBEK883615LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/73K881868LIQUID CHROMATOGRAPHY COLUMNS HISEP COLUMN & GUARDK881361SOLID PHASE EXTRACTION TUBESK880724LIQUID CHROMATO. COLUMNS

View all 24 devices →

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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