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FDA 510(k)

STAODYN EMS/PLUS

K-Number: K832988 · 1983-11-22

ApplicantStaodynamics, Inc.
Decision Date1983-11-22
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STAODYN EMS/PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Staodynamics, Inc.. It received FDA 510(k) clearance on 1983-11-22 under 510(k) number K832988. 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 STAODYN EMS/PLUS?

STAODYN EMS/PLUS is a medical device that received FDA 510(k) clearance on 1983-11-22. The listed applicant is Staodynamics, Inc.. The 510(k) number is K832988.

When did STAODYN EMS/PLUS receive FDA 510(k) clearance?

STAODYN EMS/PLUS received FDA 510(k) clearance on 1983-11-22, under 510(k) number K832988.

Who is the listed applicant for STAODYN EMS/PLUS?

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

What is the FDA product code for STAODYN EMS/PLUS?

The FDA product code for STAODYN EMS/PLUS is IPF.

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Other records listing Staodynamics, Inc. as applicant

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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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