ANGIO SYS FLUOROSCOPE DRAPE
K-Number: K843259 · 1984-09-21
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Device Summary
Frequently Asked Questions
What is the ANGIO SYS FLUOROSCOPE DRAPE?
ANGIO SYS FLUOROSCOPE DRAPE is a medical device that received FDA 510(k) clearance on 1984-09-21. The listed applicant is Angiosystems, Inc.. The 510(k) number is K843259.
When did ANGIO SYS FLUOROSCOPE DRAPE receive FDA 510(k) clearance?
ANGIO SYS FLUOROSCOPE DRAPE received FDA 510(k) clearance on 1984-09-21, under 510(k) number K843259.
Who is the listed applicant for ANGIO SYS FLUOROSCOPE DRAPE?
The FDA 510(k) record lists Angiosystems, Inc. as the applicant. This does not by itself establish the device manufacturer.
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 Angiosystems, 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.
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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