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FDA 510(k)

DILUTOR TRANSPORTER

K-Number: K780785 · 1978-06-14

ApplicantHyland Therapeutic Div., Travenol Laboratories
Decision Date1978-06-14
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DILUTOR TRANSPORTER is the device name listed in this FDA 510(k) record. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. It received FDA 510(k) clearance on 1978-06-14 under 510(k) number K780785. 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 DILUTOR TRANSPORTER?

DILUTOR TRANSPORTER is a medical device that received FDA 510(k) clearance on 1978-06-14. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. The 510(k) number is K780785.

When did DILUTOR TRANSPORTER receive FDA 510(k) clearance?

DILUTOR TRANSPORTER received FDA 510(k) clearance on 1978-06-14, under 510(k) number K780785.

Who is the listed applicant for DILUTOR TRANSPORTER?

The FDA 510(k) record lists Hyland Therapeutic Div., Travenol Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DILUTOR TRANSPORTER?

The FDA product code for DILUTOR TRANSPORTER is JQW.

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Other records listing Hyland Therapeutic Div., Travenol Laboratories as applicant

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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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