FDA 510(k)

2700 SAMPLE MANAGER

K-Number: K980180 · 1998-02-12

Decision Date1998-02-12

Product CodeJQW

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

2700 SAMPLE MANAGER is the device name listed in this FDA 510(k) record. The listed applicant is Waters Corporation. It received FDA 510(k) clearance on 1998-02-12 under 510(k) number K980180. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 2700 SAMPLE MANAGER?

2700 SAMPLE MANAGER is a medical device that received FDA 510(k) clearance on 1998-02-12. The listed applicant is Waters Corporation. The 510(k) number is K980180.

When did 2700 SAMPLE MANAGER receive FDA 510(k) clearance?

2700 SAMPLE MANAGER received FDA 510(k) clearance on 1998-02-12, under 510(k) number K980180.

Who is the listed applicant for 2700 SAMPLE MANAGER?

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 2700 SAMPLE MANAGER?

The FDA product code for 2700 SAMPLE MANAGER is JQW.

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Other records listing Waters Corporation as applicant

K063868MASSTRAK IMMUNOSUPPRESSANTS KIT K9730742487 DUAL WAVELENGTH ABSORBANCE DETECTOR K964588WATERS 515 HPLC PUMP (515)K962574WATERS 474 SCANNING FLOURESCENCE DETECTOR (474)K961557ALLIANCE 2690 SEPARATIONS MODULE

Related Devices (Code: JQW)

K023955BD VIPER INSTRUMENTBecton, Dickinson & CO K973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K970420MASTERCAP AM 5.0/MASTERCAP RM 5.0Pharmacia, Inc.K970616MINI SAMPLER PROCESSORCavro Scientific Instruments, Inc.K962687GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEMNichols Institute Diagnostics K962859MINI SAMPLE PROCESSORCavro Scientific Instruments, Inc.

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.