FDA 510(k)

CLINICAL CARE STIMULATOR

K-Number: K840725 · 1984-04-18

Decision Date1984-04-18

Product Code

DecisionSubstantially Equivalent

Device Summary

CLINICAL CARE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Biostim, Inc.. It received FDA 510(k) clearance on 1984-04-18 under 510(k) number K840725. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLINICAL CARE STIMULATOR?

CLINICAL CARE STIMULATOR is a medical device that received FDA 510(k) clearance on 1984-04-18. The listed applicant is Biostim, Inc.. The 510(k) number is K840725.

When did CLINICAL CARE STIMULATOR receive FDA 510(k) clearance?

CLINICAL CARE STIMULATOR received FDA 510(k) clearance on 1984-04-18, under 510(k) number K840725.

Who is the listed applicant for CLINICAL CARE STIMULATOR?

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

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 Biostim, Inc. as applicant

K844023AQUAFORM ELECTRODES WITH AQUAPORE K840724MUSCLE STIMULATOR X-10 K820678SYSTEM 10 K802227ANASTIM II TRANSCUTANEOUS ELECTRICAL

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.