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FDA 510(k)

DENTISCOPE

K-Number: K820907 · 1982-05-05

ApplicantChayes Virginia, Inc.
Decision Date1982-05-05
Product CodeEAY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTISCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Chayes Virginia, Inc.. It received FDA 510(k) clearance on 1982-05-05 under 510(k) number K820907. The device is classified under product code EAY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTISCOPE?

DENTISCOPE is a medical device that received FDA 510(k) clearance on 1982-05-05. The listed applicant is Chayes Virginia, Inc.. The 510(k) number is K820907.

When did DENTISCOPE receive FDA 510(k) clearance?

DENTISCOPE received FDA 510(k) clearance on 1982-05-05, under 510(k) number K820907.

Who is the listed applicant for DENTISCOPE?

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

What is the FDA product code for DENTISCOPE?

The FDA product code for DENTISCOPE is EAY.

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.

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Other records listing Chayes Virginia, 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.

K771873VISION SERIES DENTAL CHAIRK771890PERCEPTION SERIES DELIVERY SYS.K760599DENTAL CHAIRS

Related Devices (Code: EAY)

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.

K953192MODEL A15-103Beaverstate Dental, Inc.K953191MODEL A15-101Beaverstate Dental, Inc.K935718JEDENTAL VLC DENTAL CURING LIGHTJedental Co., Inc.K871816STRYKERSCOPE TM/ORTHOSCOPE TM/STRYKER MINISCOPE TMStryker Corp.K831976POWER OPTICRitter Co.K831824DENTAL ELECTRONIC/S.B.R TRADING BU HANDSilverman'S

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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