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FDA 510(k)

PERALISTIC PUMP MODEL 2000

K-Number: K780789 · 1978-06-13

ApplicantInnovative Medical Systems, Inc.
Decision Date1978-06-13
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PERALISTIC PUMP MODEL 2000 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 1978-06-13 under 510(k) number K780789. 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 PERALISTIC PUMP MODEL 2000?

PERALISTIC PUMP MODEL 2000 is a medical device that received FDA 510(k) clearance on 1978-06-13. The listed applicant is Innovative Medical Systems, Inc.. The 510(k) number is K780789.

When did PERALISTIC PUMP MODEL 2000 receive FDA 510(k) clearance?

PERALISTIC PUMP MODEL 2000 received FDA 510(k) clearance on 1978-06-13, under 510(k) number K780789.

Who is the listed applicant for PERALISTIC PUMP MODEL 2000?

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 PERALISTIC PUMP MODEL 2000?

The FDA product code for PERALISTIC PUMP MODEL 2000 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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