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FDA 510(k)

INCLINOMETER

K-Number: K954647 · 1995-10-30

ApplicantJ-Tech, Inc.
Decision Date1995-10-30
Product CodeKQX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INCLINOMETER is the device name listed in this FDA 510(k) record. The listed applicant is J-Tech, Inc.. It received FDA 510(k) clearance on 1995-10-30 under 510(k) number K954647. 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 INCLINOMETER?

INCLINOMETER is a medical device that received FDA 510(k) clearance on 1995-10-30. The listed applicant is J-Tech, Inc.. The 510(k) number is K954647.

When did INCLINOMETER receive FDA 510(k) clearance?

INCLINOMETER received FDA 510(k) clearance on 1995-10-30, under 510(k) number K954647.

Who is the listed applicant for INCLINOMETER?

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

What is the FDA product code for INCLINOMETER?

The FDA product code for INCLINOMETER is KQX.

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.

Other records listing J-Tech, 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.

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.

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.

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