PHILLIPS EASY VISION FAMILY WORKSTATION OPTION ENDO 3D
K-Number: K973983 · 1998-01-08
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Device Summary
Frequently Asked Questions
What is the PHILLIPS EASY VISION FAMILY WORKSTATION OPTION ENDO 3D?
PHILLIPS EASY VISION FAMILY WORKSTATION OPTION ENDO 3D is a medical device that received FDA 510(k) clearance on 1998-01-08. The listed applicant is Philips Medical Systems, Inc.. The 510(k) number is K973983.
When did PHILLIPS EASY VISION FAMILY WORKSTATION OPTION ENDO 3D receive FDA 510(k) clearance?
PHILLIPS EASY VISION FAMILY WORKSTATION OPTION ENDO 3D received FDA 510(k) clearance on 1998-01-08, under 510(k) number K973983.
Who is the listed applicant for PHILLIPS EASY VISION FAMILY WORKSTATION OPTION ENDO 3D?
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 PHILLIPS EASY VISION FAMILY WORKSTATION OPTION ENDO 3D?
The FDA product code for PHILLIPS EASY VISION FAMILY WORKSTATION OPTION ENDO 3D is LLZ.
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: LLZ)
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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