ANGIOGRAPHY DRAPE PACK
K-Number: K902293 · 1990-07-19
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Device Summary
Frequently Asked Questions
What is the ANGIOGRAPHY DRAPE PACK?
ANGIOGRAPHY DRAPE PACK is a medical device that received FDA 510(k) clearance on 1990-07-19. The listed applicant is Biocor Medical, Inc.. The 510(k) number is K902293.
When did ANGIOGRAPHY DRAPE PACK receive FDA 510(k) clearance?
ANGIOGRAPHY DRAPE PACK received FDA 510(k) clearance on 1990-07-19, under 510(k) number K902293.
Who is the listed applicant for ANGIOGRAPHY DRAPE PACK?
The FDA 510(k) record lists Biocor Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANGIOGRAPHY DRAPE PACK?
The FDA product code for ANGIOGRAPHY DRAPE PACK is LRO.
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 Biocor Medical, 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: LRO)
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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