MODIFIED SL-SERIES LINEAR ACCELERATORS
K-Number: K883067 · 1988-09-30
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Device Summary
Frequently Asked Questions
What is the MODIFIED SL-SERIES LINEAR ACCELERATORS?
MODIFIED SL-SERIES LINEAR ACCELERATORS is a medical device that received FDA 510(k) clearance on 1988-09-30. The listed applicant is Philips Medical Systems, Inc.. The 510(k) number is K883067.
When did MODIFIED SL-SERIES LINEAR ACCELERATORS receive FDA 510(k) clearance?
MODIFIED SL-SERIES LINEAR ACCELERATORS received FDA 510(k) clearance on 1988-09-30, under 510(k) number K883067.
Who is the listed applicant for MODIFIED SL-SERIES LINEAR ACCELERATORS?
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 MODIFIED SL-SERIES LINEAR ACCELERATORS?
The FDA product code for MODIFIED SL-SERIES LINEAR ACCELERATORS is IYE.
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: IYE)
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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