SALIVA EJECTOR
K-Number: K760620 · 1976-09-21
Advertisement
Device Summary
Frequently Asked Questions
What is the SALIVA EJECTOR?
SALIVA EJECTOR is a medical device that received FDA 510(k) clearance on 1976-09-21. The listed applicant is Lorvic Corp.. The 510(k) number is K760620.
When did SALIVA EJECTOR receive FDA 510(k) clearance?
SALIVA EJECTOR received FDA 510(k) clearance on 1976-09-21, under 510(k) number K760620.
Who is the listed applicant for SALIVA EJECTOR?
The FDA 510(k) record lists Lorvic Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SALIVA EJECTOR?
The FDA product code for SALIVA EJECTOR is DYN.
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 Lorvic Corp. 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: DYN)
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