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FDA 510(k)

JT-3 ELECTROGNATHOGRAPH

K-Number: K952218 · 1995-09-21

ApplicantBio-Research Associates, Inc.
Decision Date1995-09-21
Product CodeNFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JT-3 ELECTROGNATHOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Research Associates, Inc.. It received FDA 510(k) clearance on 1995-09-21 under 510(k) number K952218. The device is classified under product code NFS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JT-3 ELECTROGNATHOGRAPH?

JT-3 ELECTROGNATHOGRAPH is a medical device that received FDA 510(k) clearance on 1995-09-21. The listed applicant is Bio-Research Associates, Inc.. The 510(k) number is K952218.

When did JT-3 ELECTROGNATHOGRAPH receive FDA 510(k) clearance?

JT-3 ELECTROGNATHOGRAPH received FDA 510(k) clearance on 1995-09-21, under 510(k) number K952218.

Who is the listed applicant for JT-3 ELECTROGNATHOGRAPH?

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

What is the FDA product code for JT-3 ELECTROGNATHOGRAPH?

The FDA product code for JT-3 ELECTROGNATHOGRAPH is NFS.

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Other records listing Bio-Research Associates, 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.

K130158M-SCANK082927BIOEMG IIIK061799QUADRATENS, MODEL QT-42K003176BIOEMG II AND BIOJVAK9917563 CHANNEL KNEE ELECTRONIC AMPLIFIED STETHOSCOPEK981563BIOPAK MEASUREMENT SYSTEM

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Related Devices (Code: NFS)

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.

K843951SIROGNATHOGRAPHSiemens Medical Solutions USA, 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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