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FDA 510(k)

DILUTER/DISPENSER

K-Number: K780882 · 1978-06-28

ApplicantInnovative Medical Systems, Inc.
Decision Date1978-06-28
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DILUTER/DISPENSER is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Medical Systems, Inc.. It received FDA 510(k) clearance on 1978-06-28 under 510(k) number K780882. 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 DILUTER/DISPENSER?

DILUTER/DISPENSER is a medical device that received FDA 510(k) clearance on 1978-06-28. The listed applicant is Innovative Medical Systems, Inc.. The 510(k) number is K780882.

When did DILUTER/DISPENSER receive FDA 510(k) clearance?

DILUTER/DISPENSER received FDA 510(k) clearance on 1978-06-28, under 510(k) number K780882.

Who is the listed applicant for DILUTER/DISPENSER?

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

What is the FDA product code for DILUTER/DISPENSER?

The FDA product code for DILUTER/DISPENSER is JQW.

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Other records listing Innovative Medical Systems, 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.

K973035VIOLA II DENTAL CAMERA SYSTEMK951469BAZOOKA SYSTEMK933184POSITIVE AIRWAY PRESSURE SYSTEMK924590MICROWAVE AUTOMATED TISSUE PROCESSORK922081LABOTECH AUTOMATED MICROTITER ANALYZERK921005AUTOLOADER

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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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