R & D 3K RETIC
K-Number: K003208 · 2000-11-07
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Device Summary
Frequently Asked Questions
What is the R & D 3K RETIC?
R & D 3K RETIC is a medical device that received FDA 510(k) clearance on 2000-11-07. The listed applicant is R&D Systems, Inc.. The 510(k) number is K003208.
When did R & D 3K RETIC receive FDA 510(k) clearance?
R & D 3K RETIC received FDA 510(k) clearance on 2000-11-07, under 510(k) number K003208.
Who is the listed applicant for R & D 3K RETIC?
The FDA 510(k) record lists R&D Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for R & D 3K RETIC?
The FDA product code for R & D 3K RETIC is JPK.
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 R&D Systems, 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: JPK)
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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