DENTAL MOUTHPROP (BITE BLOCK)
K-Number: K792157 · 1979-11-13
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement