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FDA 510(k)

RAMVAC DENTAL VACUUM SYSTEM

K-Number: K895876 · 1989-12-26

ApplicantRamvac Corp.
Decision Date1989-12-26
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RAMVAC DENTAL VACUUM SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ramvac Corp.. It received FDA 510(k) clearance on 1989-12-26 under 510(k) number K895876. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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

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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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