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FDA 510(k)

PERLIDENT

K-Number: K894933 · 1989-10-12

ApplicantGermiphene Corp.
Decision Date1989-10-12
Product CodeEJR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERLIDENT is the device name listed in this FDA 510(k) record. The listed applicant is Germiphene Corp.. It received FDA 510(k) clearance on 1989-10-12 under 510(k) number K894933. The device is classified under product code EJR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERLIDENT?

PERLIDENT is a medical device that received FDA 510(k) clearance on 1989-10-12. The listed applicant is Germiphene Corp.. The 510(k) number is K894933.

When did PERLIDENT receive FDA 510(k) clearance?

PERLIDENT received FDA 510(k) clearance on 1989-10-12, under 510(k) number K894933.

Who is the listed applicant for PERLIDENT?

The FDA 510(k) record lists Germiphene Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERLIDENT?

The FDA product code for PERLIDENT is EJR.

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.

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Other records listing Germiphene 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.

K983847MODIFICATION OF: ODYSSEY I DENTAL WATER UNITK961289VAPOPHENEK964796ODYSSEY I DENTAL WATER UNITK942851SMILE INTEGRATED PROPHYLAXIS PASTE RINGS

Related Devices (Code: EJR)

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.

K171189AIR-FLOW PLUS Prophylaxis powderE.M.S Electro Medical Systems S.AK121698NUPRO SENSODYNE PROPHYLAXIS PASTE WITH NOVAMINDentsply International, Inc.K103114OSSPRAY SYLC CROsspray, Ltd.K102053BUTLER CALCI-FLOR PROPHYLAXIS PASTESunstar Americas, Inc.K101104REMIN PROVoco GmbHK100539PREVENTECH PROPHYLAXIS PASTE WITH FLUORIDEPreventive Technologies, Inc.

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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