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FDA 510(k)

CONSTANT CURRENT STIMULATOR MODEL 022101

K-Number: K900553 · 1990-03-13

ApplicantEp Technologies, Inc.
Decision Date1990-03-13
Product CodeJOQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CONSTANT CURRENT STIMULATOR MODEL 022101 is the device name listed in this FDA 510(k) record. The listed applicant is Ep Technologies, Inc.. It received FDA 510(k) clearance on 1990-03-13 under 510(k) number K900553. The device is classified under product code JOQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONSTANT CURRENT STIMULATOR MODEL 022101?

CONSTANT CURRENT STIMULATOR MODEL 022101 is a medical device that received FDA 510(k) clearance on 1990-03-13. The listed applicant is Ep Technologies, Inc.. The 510(k) number is K900553.

When did CONSTANT CURRENT STIMULATOR MODEL 022101 receive FDA 510(k) clearance?

CONSTANT CURRENT STIMULATOR MODEL 022101 received FDA 510(k) clearance on 1990-03-13, under 510(k) number K900553.

Who is the listed applicant for CONSTANT CURRENT STIMULATOR MODEL 022101?

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

What is the FDA product code for CONSTANT CURRENT STIMULATOR MODEL 022101?

The FDA product code for CONSTANT CURRENT STIMULATOR MODEL 022101 is JOQ.

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Other records listing Ep Technologies, 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.

K043257REAL-TIME POSITION MANAGEMENT (RPM) SYSTEMK013349ASTRONOMER PLUS SYSTEMK003452POLARIS X CATHETERS, MODEL 7000D,7001D,7003D,7004D,7005D,7006DK940167DIAGNOSTIC I CATHETERK940168DIAGNOSTIC II CATHETERK924109STEEROCATH II

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Related Devices (Code: JOQ)

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.

K173439Bloom2 Programmable Electrophysiology StimulatorFischer MedicalK092913EP-4TM CARDIAC STIMULATOR, MODELS: EP-04-02, EP-04-04Ep MedsystemsK072200STIMLABMicropace Pty, Ltd.K070743Z6 STIMULATORSt Cardio Technologies, LLCK041442EP-4 CLINICAL STIMUTATOREp MedsystemsK040207EP-4 CLINICAL STIMULATOREp Medsystems

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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