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FDA 510(k)

ELECTRODES, STAODERM STERILE

K-Number: K790542 · 1979-05-23

ApplicantStaodynamics, Inc.
Decision Date1979-05-23
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTRODES, STAODERM STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Staodynamics, Inc.. It received FDA 510(k) clearance on 1979-05-23 under 510(k) number K790542. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRODES, STAODERM STERILE?

ELECTRODES, STAODERM STERILE is a medical device that received FDA 510(k) clearance on 1979-05-23. The listed applicant is Staodynamics, Inc.. The 510(k) number is K790542.

When did ELECTRODES, STAODERM STERILE receive FDA 510(k) clearance?

ELECTRODES, STAODERM STERILE received FDA 510(k) clearance on 1979-05-23, under 510(k) number K790542.

Who is the listed applicant for ELECTRODES, STAODERM STERILE?

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 ELECTRODES, STAODERM STERILE?

The FDA product code for ELECTRODES, STAODERM STERILE is GXY.

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Other records listing Staodynamics, 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.

K852298TENS-AID STERILE ELECTRODES FOR POST-OP TENSK843964TENS-AID PREMIUM ELECTRODESK832988STAODYN EMS/PLUSK81328310D (TENS DEVICE)K813098TENS DEVICEK811345INSIGHT

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Related Devices (Code: GXY)

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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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