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FDA 510(k)

WATERS(TM) LC MODULE I FOR CLINICAL USE

K-Number: K922388 · 1992-09-11

ApplicantMillipore Corp.
Decision Date1992-09-11
Product CodeLDM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

WATERS(TM) LC MODULE I FOR CLINICAL USE is the device name listed in this FDA 510(k) record. The listed applicant is Millipore Corp.. It received FDA 510(k) clearance on 1992-09-11 under 510(k) number K922388. 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 WATERS(TM) LC MODULE I FOR CLINICAL USE?

WATERS(TM) LC MODULE I FOR CLINICAL USE is a medical device that received FDA 510(k) clearance on 1992-09-11. The listed applicant is Millipore Corp.. The 510(k) number is K922388.

When did WATERS(TM) LC MODULE I FOR CLINICAL USE receive FDA 510(k) clearance?

WATERS(TM) LC MODULE I FOR CLINICAL USE received FDA 510(k) clearance on 1992-09-11, under 510(k) number K922388.

Who is the listed applicant for WATERS(TM) LC MODULE I FOR CLINICAL USE?

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 WATERS(TM) LC MODULE I FOR CLINICAL USE?

The FDA product code for WATERS(TM) LC MODULE I FOR CLINICAL USE is LDM.

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: 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-RadK920136WATERS 717 AUTOSAMPLERMillipore Corp.K903647MODULE 486 VARIABLE WAVELENGTH TUNABLE UV/VIS DETEMillipore Corp.K884886MODEL 250 LIQUID CHROMOTAGRAPHY PUMPThe Perkin-Elmer 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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