AMERICAN ORTHOPAEDIC VACUUM 0295-250
K-Number: K861073 · 1986-03-28
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Device Summary
Frequently Asked Questions
What is the AMERICAN ORTHOPAEDIC VACUUM 0295-250?
AMERICAN ORTHOPAEDIC VACUUM 0295-250 is a medical device that received FDA 510(k) clearance on 1986-03-28. The listed applicant is Martin Medical. The 510(k) number is K861073.
When did AMERICAN ORTHOPAEDIC VACUUM 0295-250 receive FDA 510(k) clearance?
AMERICAN ORTHOPAEDIC VACUUM 0295-250 received FDA 510(k) clearance on 1986-03-28, under 510(k) number K861073.
Who is the listed applicant for AMERICAN ORTHOPAEDIC VACUUM 0295-250?
The FDA 510(k) record lists Martin Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AMERICAN ORTHOPAEDIC VACUUM 0295-250?
The FDA product code for AMERICAN ORTHOPAEDIC VACUUM 0295-250 is LGF.
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 Martin Medical 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: LGF)
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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