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FDA 510(k)

CDR-CAM

K-Number: K963778 · 1996-11-22

Decision Date1996-11-22
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CDR-CAM is the device name listed in this FDA 510(k) record. The listed applicant is Schick Technologies, Inc.. It received FDA 510(k) clearance on 1996-11-22 under 510(k) number K963778. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CDR-CAM?

CDR-CAM is a medical device that received FDA 510(k) clearance on 1996-11-22. The listed applicant is Schick Technologies, Inc.. The 510(k) number is K963778.

When did CDR-CAM receive FDA 510(k) clearance?

CDR-CAM received FDA 510(k) clearance on 1996-11-22, under 510(k) number K963778.

Who is the listed applicant for CDR-CAM?

The FDA 510(k) record lists Schick Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CDR-CAM?

The FDA product code for CDR-CAM is EIA.

Other records listing Schick Technologies, 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.

View all 13 devices →

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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