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FDA 510(k)

POINT LOCATOR STIMULATOR

K-Number: K792529 · 1980-02-26

ApplicantStaodynamics, Inc.
Decision Date1980-02-26
Product CodeBWJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POINT LOCATOR STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Staodynamics, Inc.. It received FDA 510(k) clearance on 1980-02-26 under 510(k) number K792529. The device is classified under product code BWJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POINT LOCATOR STIMULATOR?

POINT LOCATOR STIMULATOR is a medical device that received FDA 510(k) clearance on 1980-02-26. The listed applicant is Staodynamics, Inc.. The 510(k) number is K792529.

When did POINT LOCATOR STIMULATOR receive FDA 510(k) clearance?

POINT LOCATOR STIMULATOR received FDA 510(k) clearance on 1980-02-26, under 510(k) number K792529.

Who is the listed applicant for POINT LOCATOR STIMULATOR?

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 POINT LOCATOR STIMULATOR?

The FDA product code for POINT LOCATOR STIMULATOR is BWJ.

Related Clinical Trials

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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: BWJ)

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.

K792501PLS MINIStaodynamics, Inc.K772424RYUSEIErcona Corp.

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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