PM2002 CC AND PM2002 EC
K-Number: K904948 · 1991-01-30
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Device Summary
Frequently Asked Questions
What is the PM2002 CC AND PM2002 EC?
PM2002 CC AND PM2002 EC is a medical device that received FDA 510(k) clearance on 1991-01-30. The listed applicant is Planmeca USA, Inc.. The 510(k) number is K904948.
When did PM2002 CC AND PM2002 EC receive FDA 510(k) clearance?
PM2002 CC AND PM2002 EC received FDA 510(k) clearance on 1991-01-30, under 510(k) number K904948.
Who is the listed applicant for PM2002 CC AND PM2002 EC?
The FDA 510(k) record lists Planmeca USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PM2002 CC AND PM2002 EC?
The FDA product code for PM2002 CC AND PM2002 EC is EIA.
Other records listing Planmeca USA, 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: EIA)
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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