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)

SEP-PAK CARTRIDGES (LIQUID CHROMATOGRAPHY)

K-Number: K864267 · 1987-01-09

ApplicantMillipore Corp.
Decision Date1987-01-09
Product CodeDPM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SEP-PAK CARTRIDGES (LIQUID CHROMATOGRAPHY) is the device name listed in this FDA 510(k) record. The listed applicant is Millipore Corp.. It received FDA 510(k) clearance on 1987-01-09 under 510(k) number K864267. 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 SEP-PAK CARTRIDGES (LIQUID CHROMATOGRAPHY)?

SEP-PAK CARTRIDGES (LIQUID CHROMATOGRAPHY) is a medical device that received FDA 510(k) clearance on 1987-01-09. The listed applicant is Millipore Corp.. The 510(k) number is K864267.

When did SEP-PAK CARTRIDGES (LIQUID CHROMATOGRAPHY) receive FDA 510(k) clearance?

SEP-PAK CARTRIDGES (LIQUID CHROMATOGRAPHY) received FDA 510(k) clearance on 1987-01-09, under 510(k) number K864267.

Who is the listed applicant for SEP-PAK CARTRIDGES (LIQUID CHROMATOGRAPHY)?

The FDA 510(k) record lists Millipore Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEP-PAK CARTRIDGES (LIQUID CHROMATOGRAPHY)?

The FDA product code for SEP-PAK CARTRIDGES (LIQUID CHROMATOGRAPHY) 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Millipore Corp. 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.

K023892MILLEX VV, GV, AND HV SYRINGE FILTER UNITSK013988MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 RK963717MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS)K941326ULTRAFREE-CLK934069MILLEX, DUALEX (PLUS, ULTRA)K924347WATERS(TM) 996 PDA

View all 30 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.

K952501TOX PERFECT B TUBES AND REAGENTSChimera Research & Chemical, Inc.K895105HIGH PRESSURE INERT PLASTIC COLUMNS FOR CLIN. USEWaters Chemical ProductsK894141LIQUID CHROMATOGRAPHY COLUMNSSupelco, Inc.K891673ADVANCED PURIFICATION GLASS COLUMNWaters Chemical ProductsK884403LIQUID CHROMATOGRAPHY COLUMNS SOLID PHASE EX. TUBESupelco, Inc.K881868LIQUID CHROMATOGRAPHY COLUMNS HISEP COLUMN & GUARDSupelco, Inc.

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.

↑