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FDA 510(k)

HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM

K-Number: K872582 · 1987-07-16

ApplicantMillipore Corp.
Decision Date1987-07-16
Product CodeLDM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Millipore Corp.. It received FDA 510(k) clearance on 1987-07-16 under 510(k) number K872582. The device is classified under product code LDM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM?

HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM is a medical device that received FDA 510(k) clearance on 1987-07-16. The listed applicant is Millipore Corp.. The 510(k) number is K872582.

When did HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM receive FDA 510(k) clearance?

HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM received FDA 510(k) clearance on 1987-07-16, under 510(k) number K872582.

Who is the listed applicant for HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM?

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 HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM?

The FDA product code for HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM is LDM.

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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

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Related Devices (Code: LDM)

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.

K960392CDMBio-RadK961557ALLIANCE 2690 SEPARATIONS MODULEWaters CorporationK942451BIO-RAD CLINICAL DATA MANAGEMENT SYSTEMBio-RadK922388WATERS(TM) LC MODULE I FOR CLINICAL USEMillipore Corp.K920136WATERS 717 AUTOSAMPLERMillipore Corp.K903647MODULE 486 VARIABLE WAVELENGTH TUNABLE UV/VIS DETEMillipore Corp.

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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