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FDA 510(k)

DENTAL MOUTHPROP (BITE BLOCK)

K-Number: K792157 · 1979-11-13

Decision Date1979-11-13
Product CodeJXL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DENTAL MOUTHPROP (BITE BLOCK) is the device name listed in this FDA 510(k) record. The listed applicant is Mission Dental, Inc.. It received FDA 510(k) clearance on 1979-11-13 under 510(k) number K792157. The device is classified under product code JXL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL MOUTHPROP (BITE BLOCK)?

DENTAL MOUTHPROP (BITE BLOCK) is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Mission Dental, Inc.. The 510(k) number is K792157.

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

DENTAL MOUTHPROP (BITE BLOCK) received FDA 510(k) clearance on 1979-11-13, under 510(k) number K792157.

Who is the listed applicant for DENTAL MOUTHPROP (BITE BLOCK)?

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

What is the FDA product code for DENTAL MOUTHPROP (BITE BLOCK)?

The FDA product code for DENTAL MOUTHPROP (BITE BLOCK) is JXL.

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.

Other records listing Mission Dental, 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.

Related Devices (Code: JXL)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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