LP-60 LOW PRESSURE INFLATION DEVICE
K-Number: K910205 · 1991-02-25
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Device Summary
Frequently Asked Questions
What is the LP-60 LOW PRESSURE INFLATION DEVICE?
LP-60 LOW PRESSURE INFLATION DEVICE is a medical device that received FDA 510(k) clearance on 1991-02-25. The listed applicant is Devices For Vascular Intervention, Inc.. The 510(k) number is K910205.
When did LP-60 LOW PRESSURE INFLATION DEVICE receive FDA 510(k) clearance?
LP-60 LOW PRESSURE INFLATION DEVICE received FDA 510(k) clearance on 1991-02-25, under 510(k) number K910205.
Who is the listed applicant for LP-60 LOW PRESSURE INFLATION DEVICE?
The FDA 510(k) record lists Devices For Vascular Intervention, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LP-60 LOW PRESSURE INFLATION DEVICE?
The FDA product code for LP-60 LOW PRESSURE INFLATION DEVICE is MAV.
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 Devices For Vascular Intervention, 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: MAV)
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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