ALTERNATING PRESSURE PUMP AND PAD SYSTEM
K-Number: K900871 · 1990-04-04
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Device Summary
Frequently Asked Questions
What is the ALTERNATING PRESSURE PUMP AND PAD SYSTEM?
ALTERNATING PRESSURE PUMP AND PAD SYSTEM is a medical device that received FDA 510(k) clearance on 1990-04-04. The listed applicant is Three Bears Intl.. The 510(k) number is K900871.
When did ALTERNATING PRESSURE PUMP AND PAD SYSTEM receive FDA 510(k) clearance?
ALTERNATING PRESSURE PUMP AND PAD SYSTEM received FDA 510(k) clearance on 1990-04-04, under 510(k) number K900871.
Who is the listed applicant for ALTERNATING PRESSURE PUMP AND PAD SYSTEM?
The FDA 510(k) record lists Three Bears Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALTERNATING PRESSURE PUMP AND PAD SYSTEM?
The FDA product code for ALTERNATING PRESSURE PUMP AND PAD SYSTEM is FNM.
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.
Related Devices (Code: FNM)
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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