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FDA 510(k)

CEREC 2

K-Number: K950299 · 1995-05-23

Decision Date1995-05-23
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CEREC 2 is the device name listed in this FDA 510(k) record. The listed applicant is Pelton & Crane Co.. It received FDA 510(k) clearance on 1995-05-23 under 510(k) number K950299. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 14 devices →

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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