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FDA 510(k)

STRESS MACHINE

K-Number: K831699 · 1983-07-12

ApplicantDr. William F. Curran
Decision Date1983-07-12
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STRESS MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Dr. William F. Curran. It received FDA 510(k) clearance on 1983-07-12 under 510(k) number K831699. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRESS MACHINE?

STRESS MACHINE is a medical device that received FDA 510(k) clearance on 1983-07-12. The listed applicant is Dr. William F. Curran. The 510(k) number is K831699.

When did STRESS MACHINE receive FDA 510(k) clearance?

STRESS MACHINE received FDA 510(k) clearance on 1983-07-12, under 510(k) number K831699.

Who is the listed applicant for STRESS MACHINE?

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

What is the FDA product code for STRESS MACHINE?

The FDA product code for STRESS MACHINE is ISA.

Related Clinical Trials

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Related Devices (Code: ISA)

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.

K243488VMAT PROTermosaludK240358ShockPhysio Mobile (model SW3200 Basic)Shenzhen Dongdixin Technology Co., Ltd.K221865BTL-094BTL Industries, Inc.K210166Omnispec ED1000Medispec, Ltd.K213120OW100S (model OW100S-US)Tissue Regeneration Technologies, LLC Dba AS Softwave TrtK220538DolorClast RadialE.M.S Electro Medical Systems S.A

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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