CEREC 2
K-Number: K950299 · 1995-05-23
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Device Summary
Frequently Asked Questions
What is the CEREC 2?
CEREC 2 is a medical device that received FDA 510(k) clearance on 1995-05-23. The listed applicant is Pelton & Crane Co.. The 510(k) number is K950299.
When did CEREC 2 receive FDA 510(k) clearance?
CEREC 2 received FDA 510(k) clearance on 1995-05-23, under 510(k) number K950299.
Who is the listed applicant for CEREC 2?
The FDA 510(k) record lists Pelton & Crane Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CEREC 2?
The FDA product code for CEREC 2 is ELW.
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 Pelton & Crane Co. 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: ELW)
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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