PICKER MR WORKSTATIONS (VISTAR,MONTAGE AND ONCALL)
K-Number: K961637 · 1996-07-03
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Device Summary
Frequently Asked Questions
What is the PICKER MR WORKSTATIONS (VISTAR,MONTAGE AND ONCALL)?
PICKER MR WORKSTATIONS (VISTAR,MONTAGE AND ONCALL) is a medical device that received FDA 510(k) clearance on 1996-07-03. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K961637.
When did PICKER MR WORKSTATIONS (VISTAR,MONTAGE AND ONCALL) receive FDA 510(k) clearance?
PICKER MR WORKSTATIONS (VISTAR,MONTAGE AND ONCALL) received FDA 510(k) clearance on 1996-07-03, under 510(k) number K961637.
Who is the listed applicant for PICKER MR WORKSTATIONS (VISTAR,MONTAGE AND ONCALL)?
The FDA 510(k) record lists Philips Medical Systems (Cleveland), Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PICKER MR WORKSTATIONS (VISTAR,MONTAGE AND ONCALL)?
The FDA product code for PICKER MR WORKSTATIONS (VISTAR,MONTAGE AND ONCALL) 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 (Cleveland), 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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