PHILIPS GYROSCAN TN5 & TN5 LITE
K-Number: K932644 · 1993-12-13
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Device Summary
Frequently Asked Questions
What is the PHILIPS GYROSCAN TN5 & TN5 LITE?
PHILIPS GYROSCAN TN5 & TN5 LITE is a medical device that received FDA 510(k) clearance on 1993-12-13. The listed applicant is Philips Medical Systems, Inc.. The 510(k) number is K932644.
When did PHILIPS GYROSCAN TN5 & TN5 LITE receive FDA 510(k) clearance?
PHILIPS GYROSCAN TN5 & TN5 LITE received FDA 510(k) clearance on 1993-12-13, under 510(k) number K932644.
Who is the listed applicant for PHILIPS GYROSCAN TN5 & TN5 LITE?
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 PHILIPS GYROSCAN TN5 & TN5 LITE?
The FDA product code for PHILIPS GYROSCAN TN5 & TN5 LITE 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.
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.
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