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FDA 510(k)

PIPETTING DEVICES

K-Number: K770013 · 1977-01-25

ApplicantKensington Scientific
Decision Date1977-01-25
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PIPETTING DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Kensington Scientific. It received FDA 510(k) clearance on 1977-01-25 under 510(k) number K770013. 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 PIPETTING DEVICES?

PIPETTING DEVICES is a medical device that received FDA 510(k) clearance on 1977-01-25. The listed applicant is Kensington Scientific. The 510(k) number is K770013.

When did PIPETTING DEVICES receive FDA 510(k) clearance?

PIPETTING DEVICES received FDA 510(k) clearance on 1977-01-25, under 510(k) number K770013.

Who is the listed applicant for PIPETTING DEVICES?

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

What is the FDA product code for PIPETTING DEVICES?

The FDA product code for PIPETTING DEVICES is JQW.

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 Kensington Scientific 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.

K770208MOTORIZED OPERATOR FOR PIPETTING DEV.

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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