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FDA 510(k)

CDR - PAN MODEL 4700

K-Number: K982661 · 1998-12-11

ApplicantSchick Technologies, Inc.
Decision Date1998-12-11
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CDR - PAN MODEL 4700 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 1998-12-11 under 510(k) number K982661. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CDR - PAN MODEL 4700?

CDR - PAN MODEL 4700 is a medical device that received FDA 510(k) clearance on 1998-12-11. The listed applicant is Schick Technologies, Inc.. The 510(k) number is K982661.

When did CDR - PAN MODEL 4700 receive FDA 510(k) clearance?

CDR - PAN MODEL 4700 received FDA 510(k) clearance on 1998-12-11, under 510(k) number K982661.

Who is the listed applicant for CDR - PAN MODEL 4700?

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 - PAN MODEL 4700?

The FDA product code for CDR - PAN MODEL 4700 is MQB.

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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.

K110768COMPUTED DENTAL RADIOGRAPHYK093453MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEMK072134SCHICK COMPUTED ORAL RADIOLOGY SYSTEMK053558CEPH, MODEL 4900K041385MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEMK031291CDR PANX, MODEL 4792

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Related Devices (Code: MQB)

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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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