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FDA 510(k)

BOND ELUT COLUMNS

K-Number: K800061 · 1980-03-12

ApplicantAnalytichem International, Inc.
Decision Date1980-03-12
Product CodeDJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BOND ELUT COLUMNS is the device name listed in this FDA 510(k) record. The listed applicant is Analytichem International, Inc.. It received FDA 510(k) clearance on 1980-03-12 under 510(k) number K800061. The device is classified under product code DJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOND ELUT COLUMNS?

BOND ELUT COLUMNS is a medical device that received FDA 510(k) clearance on 1980-03-12. The listed applicant is Analytichem International, Inc.. The 510(k) number is K800061.

When did BOND ELUT COLUMNS receive FDA 510(k) clearance?

BOND ELUT COLUMNS received FDA 510(k) clearance on 1980-03-12, under 510(k) number K800061.

Who is the listed applicant for BOND ELUT COLUMNS?

The FDA 510(k) record lists Analytichem International, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BOND ELUT COLUMNS?

The FDA product code for BOND ELUT COLUMNS is DJY.

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.

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Other records listing Analytichem International, 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.

K781728EXTUBE

Related Devices (Code: DJY)

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.

K890113THE CDI(R) SYSTEM 400Cardiovascular Devices, Inc.K883615LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/73Supelco, Inc.K881361SOLID PHASE EXTRACTION TUBESSupelco, Inc.K850963DUPONT PREP TYPE SI EXTRACITON CARTRIDGEE.I. Dupont DE Nemours & Co., Inc.K840985TRISACRYL GF 05 & TRISACRYL GF 2000Lkb Instruments, Inc.K832198HC40/HC75 PREPACKED COLUMSHamilton Co.

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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