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FDA 510(k)

DIGITAL ELECTRONIC MYO-GRAPH (MUSCLE ANALYZER)

K-Number: K862128 · 1986-07-11

ApplicantHealth Products, Inc.
Decision Date1986-07-11
Product CodeKQX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DIGITAL ELECTRONIC MYO-GRAPH (MUSCLE ANALYZER) is the device name listed in this FDA 510(k) record. The listed applicant is Health Products, Inc.. It received FDA 510(k) clearance on 1986-07-11 under 510(k) number K862128. The device is classified under product code KQX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL ELECTRONIC MYO-GRAPH (MUSCLE ANALYZER)?

DIGITAL ELECTRONIC MYO-GRAPH (MUSCLE ANALYZER) is a medical device that received FDA 510(k) clearance on 1986-07-11. The listed applicant is Health Products, Inc.. The 510(k) number is K862128.

When did DIGITAL ELECTRONIC MYO-GRAPH (MUSCLE ANALYZER) receive FDA 510(k) clearance?

DIGITAL ELECTRONIC MYO-GRAPH (MUSCLE ANALYZER) received FDA 510(k) clearance on 1986-07-11, under 510(k) number K862128.

Who is the listed applicant for DIGITAL ELECTRONIC MYO-GRAPH (MUSCLE ANALYZER)?

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

What is the FDA product code for DIGITAL ELECTRONIC MYO-GRAPH (MUSCLE ANALYZER)?

The FDA product code for DIGITAL ELECTRONIC MYO-GRAPH (MUSCLE ANALYZER) is KQX.

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Other records listing Health Products, 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.

K912866PEAK EXPIRATORY FLOW METERK912943THRESHOLD 2X INSPIRATORY MUSCLE TRAINERK911807METERED DOSE INHALER (MDI) SPACERK902292MODIFIED ASSESS(R) PEAK FLOW METERK896953MODIFIED ASSESS(R) PEAK FLOW METERK894353ORTHODERM CONVERTIBLE

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Related Devices (Code: KQX)

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.

K011827ORTELIUS 800Orthoscan , Ltd.K971079INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWAREInterlogics, Inc.K9623773D-SPINESkill Technologies, Inc.K961212SPINAL TOUCHFasstechK954647INCLINOMETERJ-Tech, Inc.K943929DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)Greenleaf Medical Systems, Inc.

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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