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FDA 510(k)

DELUXE WALL-MOUNTED CEPHALOMETER

K-Number: K834559 · 1984-02-21

ApplicantKnochen Dental Laboratory
Decision Date1984-02-21
Product CodeIWY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DELUXE WALL-MOUNTED CEPHALOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Knochen Dental Laboratory. It received FDA 510(k) clearance on 1984-02-21 under 510(k) number K834559. The device is classified under product code IWY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELUXE WALL-MOUNTED CEPHALOMETER?

DELUXE WALL-MOUNTED CEPHALOMETER is a medical device that received FDA 510(k) clearance on 1984-02-21. The listed applicant is Knochen Dental Laboratory. The 510(k) number is K834559.

When did DELUXE WALL-MOUNTED CEPHALOMETER receive FDA 510(k) clearance?

DELUXE WALL-MOUNTED CEPHALOMETER received FDA 510(k) clearance on 1984-02-21, under 510(k) number K834559.

Who is the listed applicant for DELUXE WALL-MOUNTED CEPHALOMETER?

The FDA 510(k) record lists Knochen Dental Laboratory as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DELUXE WALL-MOUNTED CEPHALOMETER?

The FDA product code for DELUXE WALL-MOUNTED CEPHALOMETER is IWY.

Related Clinical Trials

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Other records listing Knochen Dental Laboratory 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.

K834606X-RAY COLLIMATOR X-CJD

Related Devices (Code: IWY)

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.

K925705ACCURAD-200 SYSTEM & ACCURAD-300 PLUS SYSTEMDenar Corp.K884493HEAD HOLDING DEVICE/SLEEP APNEAX-Ray SystemsK884847MTD HEDRESTComposites Horizons, Inc.K864527DUOCEPHGary E. Hall, DdsK850197KELLER CEPHALOMETRIC DEVICEGary D. KellerK844549HEAD-SPINE STABILIZER HSS-1Imaging Accessories, Inc.

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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