Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LIQUID CHROMATOGRAPHY COLUMNS SOLID PHASE EX. TUBE

K-Number: K884403 · 1988-12-22

ApplicantSupelco, Inc.
Decision Date1988-12-22
Product CodeDPM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUID CHROMATOGRAPHY COLUMNS SOLID PHASE EX. TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Supelco, Inc.. It received FDA 510(k) clearance on 1988-12-22 under 510(k) number K884403. The device is classified under product code DPM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUID CHROMATOGRAPHY COLUMNS SOLID PHASE EX. TUBE?

LIQUID CHROMATOGRAPHY COLUMNS SOLID PHASE EX. TUBE is a medical device that received FDA 510(k) clearance on 1988-12-22. The listed applicant is Supelco, Inc.. The 510(k) number is K884403.

When did LIQUID CHROMATOGRAPHY COLUMNS SOLID PHASE EX. TUBE receive FDA 510(k) clearance?

LIQUID CHROMATOGRAPHY COLUMNS SOLID PHASE EX. TUBE received FDA 510(k) clearance on 1988-12-22, under 510(k) number K884403.

Who is the listed applicant for LIQUID CHROMATOGRAPHY COLUMNS SOLID PHASE EX. TUBE?

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 COLUMNS SOLID PHASE EX. TUBE?

The FDA product code for LIQUID CHROMATOGRAPHY COLUMNS SOLID PHASE EX. TUBE 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.

View all 24 devices →

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.

↑