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FDA 510(k)

MARK 5 ROBOTIC PIPETTOR

K-Number: K912228 · 1991-06-06

ApplicantDiagnostic Products Corp.
Decision Date1991-06-06
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MARK 5 ROBOTIC PIPETTOR is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Products Corp.. It received FDA 510(k) clearance on 1991-06-06 under 510(k) number K912228. 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 MARK 5 ROBOTIC PIPETTOR?

MARK 5 ROBOTIC PIPETTOR is a medical device that received FDA 510(k) clearance on 1991-06-06. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K912228.

When did MARK 5 ROBOTIC PIPETTOR receive FDA 510(k) clearance?

MARK 5 ROBOTIC PIPETTOR received FDA 510(k) clearance on 1991-06-06, under 510(k) number K912228.

Who is the listed applicant for MARK 5 ROBOTIC PIPETTOR?

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

What is the FDA product code for MARK 5 ROBOTIC PIPETTOR?

The FDA product code for MARK 5 ROBOTIC PIPETTOR is JQW.

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Other records listing Diagnostic Products 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.

K063045IMMULITE 2000, IMMULITE 2500 VANCOMYCINK034055IMMULITE 2500 CK-MB, 2500 MYOGLOBIN, 2500 STAT TROPONIN IK033234IMMULITE 2500 AUTOMATED IMMUNOASSAY ANALYZERK032881IMMULITE/IMMULITE 1000 TOTAL TESTOSTERONE AND IMMULITE 2000 TOTAL TESTOSTERONEK023152IMMULITE 2000 ALLERGEN-SPECIFIC IGEK023304IMMULITE/IMMULITE 1000 CALCITONIN, MODEL LKCL AND IMMULITE 2000 CALCITONIN, MODEL L2KCL

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Related Devices (Code: JQW)

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.

K023955BD VIPER INSTRUMENTBecton, Dickinson & COK973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters CorporationK970420MASTERCAP 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

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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