CONVAID CRUISER CP4M
K-Number: K810676 · 1981-03-26
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Device Summary
Frequently Asked Questions
What is the CONVAID CRUISER CP4M?
CONVAID CRUISER CP4M is a medical device that received FDA 510(k) clearance on 1981-03-26. The listed applicant is Convaid Products, Inc.. The 510(k) number is K810676.
When did CONVAID CRUISER CP4M receive FDA 510(k) clearance?
CONVAID CRUISER CP4M received FDA 510(k) clearance on 1981-03-26, under 510(k) number K810676.
Who is the listed applicant for CONVAID CRUISER CP4M?
The FDA 510(k) record lists Convaid Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONVAID CRUISER CP4M?
The FDA product code for CONVAID CRUISER CP4M is LBE.
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 Convaid Products, 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: LBE)
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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