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FDA 510(k)

JTECH COMMANDER AND ALGOMETER

K-Number: K971407 · 1998-04-20

ApplicantJ-Tech Medical, Inc.
Decision Date1998-04-20
Product CodeHRW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

JTECH COMMANDER AND ALGOMETER is the device name listed in this FDA 510(k) record. The listed applicant is J-Tech Medical, Inc.. It received FDA 510(k) clearance on 1998-04-20 under 510(k) number K971407. The device is classified under product code HRW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JTECH COMMANDER AND ALGOMETER?

JTECH COMMANDER AND ALGOMETER is a medical device that received FDA 510(k) clearance on 1998-04-20. The listed applicant is J-Tech Medical, Inc.. The 510(k) number is K971407.

When did JTECH COMMANDER AND ALGOMETER receive FDA 510(k) clearance?

JTECH COMMANDER AND ALGOMETER received FDA 510(k) clearance on 1998-04-20, under 510(k) number K971407.

Who is the listed applicant for JTECH COMMANDER AND ALGOMETER?

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

What is the FDA product code for JTECH COMMANDER AND ALGOMETER?

The FDA product code for JTECH COMMANDER AND ALGOMETER is HRW.

Related Clinical Trials

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Other records listing J-Tech Medical, 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.

K974376JTECH ADJUSTER REFLEX GUN

Related Devices (Code: HRW)

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.

K970870DIGIT-GRIP WITH LCD (DGR002)Nk Biotechnical Corp.K894557LIGHTSCOPE SETOptikK861396HANDHELD DYNAMOMETER, MODEL #160 AND #111Spark Instruments & Academics, Inc.K821631PINCH GAUGE, 0-301 LBS.Fred Sammons, Inc.K812343PINCH METERFred Sammons, Inc.K801719BK-7531 PAIN THRESHOLD/FINGER FORCE GAUGFred Sammons, 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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