INOVO, INC. ACCUPULSE SINGLE LUMEN CONSERVING REGULATOR
K-Number: K060751 · 2006-07-18
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Device Summary
Frequently Asked Questions
What is the INOVO, INC. ACCUPULSE SINGLE LUMEN CONSERVING REGULATOR?
INOVO, INC. ACCUPULSE SINGLE LUMEN CONSERVING REGULATOR is a medical device that received FDA 510(k) clearance on 2006-07-18. The listed applicant is Inovo, Inc.. The 510(k) number is K060751.
When did INOVO, INC. ACCUPULSE SINGLE LUMEN CONSERVING REGULATOR receive FDA 510(k) clearance?
INOVO, INC. ACCUPULSE SINGLE LUMEN CONSERVING REGULATOR received FDA 510(k) clearance on 2006-07-18, under 510(k) number K060751.
Who is the listed applicant for INOVO, INC. ACCUPULSE SINGLE LUMEN CONSERVING REGULATOR?
The FDA 510(k) record lists Inovo, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INOVO, INC. ACCUPULSE SINGLE LUMEN CONSERVING REGULATOR?
The FDA product code for INOVO, INC. ACCUPULSE SINGLE LUMEN CONSERVING REGULATOR is NFB.
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 Inovo, 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: NFB)
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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