FDA 510(k)

ALLIANCE 2690 SEPARATIONS MODULE

K-Number: K961557 · 1996-07-05

Decision Date1996-07-05

Product CodeLDM

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

ALLIANCE 2690 SEPARATIONS MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Waters Corporation. It received FDA 510(k) clearance on 1996-07-05 under 510(k) number K961557. 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 ALLIANCE 2690 SEPARATIONS MODULE?

ALLIANCE 2690 SEPARATIONS MODULE is a medical device that received FDA 510(k) clearance on 1996-07-05. The listed applicant is Waters Corporation. The 510(k) number is K961557.

When did ALLIANCE 2690 SEPARATIONS MODULE receive FDA 510(k) clearance?

ALLIANCE 2690 SEPARATIONS MODULE received FDA 510(k) clearance on 1996-07-05, under 510(k) number K961557.

Who is the listed applicant for ALLIANCE 2690 SEPARATIONS MODULE?

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

What is the FDA product code for ALLIANCE 2690 SEPARATIONS MODULE?

The FDA product code for ALLIANCE 2690 SEPARATIONS MODULE 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.

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Other records listing Waters Corporation as applicant

K063868MASSTRAK IMMUNOSUPPRESSANTS KIT K9801802700 SAMPLE MANAGER K9730742487 DUAL WAVELENGTH ABSORBANCE DETECTOR K964588WATERS 515 HPLC PUMP (515)K962574WATERS 474 SCANNING FLOURESCENCE DETECTOR (474)

Related Devices (Code: LDM)

K960392CDMBio-Rad K942451BIO-RAD CLINICAL DATA MANAGEMENT SYSTEMBio-Rad K922388WATERS(TM) LC MODULE I FOR CLINICAL USEMillipore Corp.K920136WATERS 717 AUTOSAMPLERMillipore Corp.K903647MODULE 486 VARIABLE WAVELENGTH TUNABLE UV/VIS DETEMillipore Corp.K884886MODEL 250 LIQUID CHROMOTAGRAPHY PUMPThe Perkin-Elmer Corp.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.