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FDA 510(k)

STIMULATOR, PNEUMATIC

K-Number: K760214 · 1977-01-21

ApplicantO. F. Anderson
Decision Date1977-01-21
Product Code
DecisionSubstantially Equivalent

Device Summary

STIMULATOR, PNEUMATIC is the device name listed in this FDA 510(k) record. The listed applicant is O. F. Anderson. It received FDA 510(k) clearance on 1977-01-21 under 510(k) number K760214. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STIMULATOR, PNEUMATIC?

STIMULATOR, PNEUMATIC is a medical device that received FDA 510(k) clearance on 1977-01-21. The listed applicant is O. F. Anderson. The 510(k) number is K760214.

When did STIMULATOR, PNEUMATIC receive FDA 510(k) clearance?

STIMULATOR, PNEUMATIC received FDA 510(k) clearance on 1977-01-21, under 510(k) number K760214.

Who is the listed applicant for STIMULATOR, PNEUMATIC?

The FDA 510(k) record lists O. F. Anderson as the applicant. This does not by itself establish the device manufacturer.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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