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FDA 510(k)

RAMCLEAN DENTAL VACUUM LINE CLEANER

K-Number: K895877 · 1989-12-26

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

Device Summary

RAMCLEAN DENTAL VACUUM LINE CLEANER 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 K895877. 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 RAMCLEAN DENTAL VACUUM LINE CLEANER?

RAMCLEAN DENTAL VACUUM LINE CLEANER 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 K895877.

When did RAMCLEAN DENTAL VACUUM LINE CLEANER receive FDA 510(k) clearance?

RAMCLEAN DENTAL VACUUM LINE CLEANER received FDA 510(k) clearance on 1989-12-26, under 510(k) number K895877.

Who is the listed applicant for RAMCLEAN DENTAL VACUUM LINE CLEANER?

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 RAMCLEAN DENTAL VACUUM LINE CLEANER?

The FDA product code for RAMCLEAN DENTAL VACUUM LINE CLEANER 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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