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FDA 510(k)

AIR DISPLACEMENT PIPETTE

K-Number: K885340 · 1989-02-14

ApplicantUlster Scientific, Inc.
Decision Date1989-02-14
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AIR DISPLACEMENT PIPETTE is the device name listed in this FDA 510(k) record. The listed applicant is Ulster Scientific, Inc.. It received FDA 510(k) clearance on 1989-02-14 under 510(k) number K885340. 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 AIR DISPLACEMENT PIPETTE?

AIR DISPLACEMENT PIPETTE is a medical device that received FDA 510(k) clearance on 1989-02-14. The listed applicant is Ulster Scientific, Inc.. The 510(k) number is K885340.

When did AIR DISPLACEMENT PIPETTE receive FDA 510(k) clearance?

AIR DISPLACEMENT PIPETTE received FDA 510(k) clearance on 1989-02-14, under 510(k) number K885340.

Who is the listed applicant for AIR DISPLACEMENT PIPETTE?

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

What is the FDA product code for AIR DISPLACEMENT PIPETTE?

The FDA product code for AIR DISPLACEMENT PIPETTE is JQW.

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Other records listing Ulster Scientific, Inc. 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.

K942620FEATHER-TOUCH SINGLE-STICK DEVICEK920562UNISTIKK902592EPC ELECTRONIC PIPETTING SYSTEMK895890AUTOPENK894474THE AUTOLET LITEK875354UNISTEP CAPILLARY BLOOD COLLECTION SYSTEM

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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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