Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

GYROSCAN T10-NT (RELEASE 4 SERIES SOFTWARE)

K-Number: K940534 · 1994-11-22

Decision Date1994-11-22
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GYROSCAN T10-NT (RELEASE 4 SERIES SOFTWARE) is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems, Inc.. It received FDA 510(k) clearance on 1994-11-22 under 510(k) number K940534. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GYROSCAN T10-NT (RELEASE 4 SERIES SOFTWARE)?

GYROSCAN T10-NT (RELEASE 4 SERIES SOFTWARE) is a medical device that received FDA 510(k) clearance on 1994-11-22. The listed applicant is Philips Medical Systems, Inc.. The 510(k) number is K940534.

When did GYROSCAN T10-NT (RELEASE 4 SERIES SOFTWARE) receive FDA 510(k) clearance?

GYROSCAN T10-NT (RELEASE 4 SERIES SOFTWARE) received FDA 510(k) clearance on 1994-11-22, under 510(k) number K940534.

Who is the listed applicant for GYROSCAN T10-NT (RELEASE 4 SERIES SOFTWARE)?

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

What is the FDA product code for GYROSCAN T10-NT (RELEASE 4 SERIES SOFTWARE)?

The FDA product code for GYROSCAN T10-NT (RELEASE 4 SERIES SOFTWARE) is LNH.

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 Philips Medical Systems, 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.

View all 111 devices →

Related Devices (Code: LNH)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑