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FDA 510(k)

BITE BLOCK SYSTEM

K-Number: K800760 · 1980-05-28

ApplicantRadiation Products Design, Inc.
Decision Date1980-05-28
Product Code
DecisionSubstantially Equivalent

Device Summary

BITE BLOCK SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Radiation Products Design, Inc.. It received FDA 510(k) clearance on 1980-05-28 under 510(k) number K800760. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BITE BLOCK SYSTEM?

BITE BLOCK SYSTEM is a medical device that received FDA 510(k) clearance on 1980-05-28. The listed applicant is Radiation Products Design, Inc.. The 510(k) number is K800760.

When did BITE BLOCK SYSTEM receive FDA 510(k) clearance?

BITE BLOCK SYSTEM received FDA 510(k) clearance on 1980-05-28, under 510(k) number K800760.

Who is the listed applicant for BITE BLOCK SYSTEM?

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

Related Clinical Trials

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Other records listing Radiation Products Design, 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.

K800761POINT TO POINT LEVELK800792ADJUSTABLE HEAD & FACE HOLDERK800790TENNIS RACKET-TABLE INSERT PANELK800759ELEV. BACK SUPPORT W/ADJ. ARM POSITIONERK800791MYLAR WINDOW-TABLE INSERT PANELK791178MYVACET 5-07, 7-00 AND 9-40

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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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