SALIVA EJECTORS
K-Number: K863768 · 1986-10-27
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Device Summary
Frequently Asked Questions
What is the SALIVA EJECTORS?
SALIVA EJECTORS is a medical device that received FDA 510(k) clearance on 1986-10-27. The listed applicant is The Medical Group, Inc.. The 510(k) number is K863768.
When did SALIVA EJECTORS receive FDA 510(k) clearance?
SALIVA EJECTORS received FDA 510(k) clearance on 1986-10-27, under 510(k) number K863768.
Who is the listed applicant for SALIVA EJECTORS?
The FDA 510(k) record lists The Medical Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SALIVA EJECTORS?
The FDA product code for SALIVA EJECTORS 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 The Medical Group, 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: 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.
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