DATASCOPE MULTINEX ID PLUS
K-Number: K930303 · 1993-06-16
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Device Summary
Frequently Asked Questions
What is the DATASCOPE MULTINEX ID PLUS?
DATASCOPE MULTINEX ID PLUS is a medical device that received FDA 510(k) clearance on 1993-06-16. The listed applicant is Datascope Corp.. The 510(k) number is K930303.
When did DATASCOPE MULTINEX ID PLUS receive FDA 510(k) clearance?
DATASCOPE MULTINEX ID PLUS received FDA 510(k) clearance on 1993-06-16, under 510(k) number K930303.
Who is the listed applicant for DATASCOPE MULTINEX ID PLUS?
The FDA 510(k) record lists Datascope Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DATASCOPE MULTINEX ID PLUS?
The FDA product code for DATASCOPE MULTINEX ID PLUS is CBQ.
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 Datascope Corp. 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: CBQ)
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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