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FDA 510(k)

EMS 300 MUSCLE STIMULATORS

K-Number: K890434 · 1989-10-17

ApplicantParanamics, Inc.
Decision Date1989-10-17
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EMS 300 MUSCLE STIMULATORS is the device name listed in this FDA 510(k) record. The listed applicant is Paranamics, Inc.. It received FDA 510(k) clearance on 1989-10-17 under 510(k) number K890434. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMS 300 MUSCLE STIMULATORS?

EMS 300 MUSCLE STIMULATORS is a medical device that received FDA 510(k) clearance on 1989-10-17. The listed applicant is Paranamics, Inc.. The 510(k) number is K890434.

When did EMS 300 MUSCLE STIMULATORS receive FDA 510(k) clearance?

EMS 300 MUSCLE STIMULATORS received FDA 510(k) clearance on 1989-10-17, under 510(k) number K890434.

Who is the listed applicant for EMS 300 MUSCLE STIMULATORS?

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

What is the FDA product code for EMS 300 MUSCLE STIMULATORS?

The FDA product code for EMS 300 MUSCLE STIMULATORS is IPF.

Related Clinical Trials

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.

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Other records listing Paranamics, 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.

K902371HAELAN 340 MUSCLE STIMULATOR

Related Devices (Code: IPF)

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.

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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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