RAMVAC DENTAL VACUUM SYSTEM
K-Number: K895876 · 1989-12-26
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Device Summary
Frequently Asked Questions
What is the RAMVAC DENTAL VACUUM SYSTEM?
RAMVAC DENTAL VACUUM SYSTEM is a medical device that received FDA 510(k) clearance on 1989-12-26. The listed applicant is Ramvac Corp.. The 510(k) number is K895876.
When did RAMVAC DENTAL VACUUM SYSTEM receive FDA 510(k) clearance?
RAMVAC DENTAL VACUUM SYSTEM received FDA 510(k) clearance on 1989-12-26, under 510(k) number K895876.
Who is the listed applicant for RAMVAC DENTAL VACUUM SYSTEM?
The FDA 510(k) record lists Ramvac Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RAMVAC DENTAL VACUUM SYSTEM?
The FDA product code for RAMVAC DENTAL VACUUM SYSTEM is EIA.
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 Ramvac 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: EIA)
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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