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FDA 510(k)

ADJUSTABLE DISPENSOR

K-Number: K780912 · 1978-06-28

ApplicantOxford Laboratories, Inc.
Decision Date1978-06-28
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ADJUSTABLE DISPENSOR is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Laboratories, Inc.. It received FDA 510(k) clearance on 1978-06-28 under 510(k) number K780912. 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 ADJUSTABLE DISPENSOR?

ADJUSTABLE DISPENSOR is a medical device that received FDA 510(k) clearance on 1978-06-28. The listed applicant is Oxford Laboratories, Inc.. The 510(k) number is K780912.

When did ADJUSTABLE DISPENSOR receive FDA 510(k) clearance?

ADJUSTABLE DISPENSOR received FDA 510(k) clearance on 1978-06-28, under 510(k) number K780912.

Who is the listed applicant for ADJUSTABLE DISPENSOR?

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

What is the FDA product code for ADJUSTABLE DISPENSOR?

The FDA product code for ADJUSTABLE DISPENSOR is JQW.

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Other records listing Oxford Laboratories, 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.

K760079REAGENT, THYROXINE T4 (#210)K760144SERUM, HAPTOGLOBIN GOAT ANTI-HUMAN ACIDK760148SERUM, B1A GLOBULIN C3C GOAT ANTI-HUMANK760078REAGENT, RIA TRIIODOTHYRONINE T3 (#200)K760143SERUM, ALPHA-1-GLYCOPROTEIN ANTI-HUMANK760146SERUM, IGA GOAT ANTI-HUMAN ACID

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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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