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FDA 510(k)

DENTAL RUBBERDAM

K-Number: K833610 · 1984-01-10

ApplicantCenter For Marketing Services
Decision Date1984-01-10
Product CodeEIE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL RUBBERDAM is the device name listed in this FDA 510(k) record. The listed applicant is Center For Marketing Services. It received FDA 510(k) clearance on 1984-01-10 under 510(k) number K833610. The device is classified under product code EIE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL RUBBERDAM?

DENTAL RUBBERDAM is a medical device that received FDA 510(k) clearance on 1984-01-10. The listed applicant is Center For Marketing Services. The 510(k) number is K833610.

When did DENTAL RUBBERDAM receive FDA 510(k) clearance?

DENTAL RUBBERDAM received FDA 510(k) clearance on 1984-01-10, under 510(k) number K833610.

Who is the listed applicant for DENTAL RUBBERDAM?

The FDA 510(k) record lists Center For Marketing Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DENTAL RUBBERDAM?

The FDA product code for DENTAL RUBBERDAM is EIE.

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Related Devices (Code: EIE)

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.

K182118armor LCMavrik Dental Systems, Ltd.K151945Triumph Resin DamDenali CorporationK050318BARI-KAD PACKING DEVICEBioenvelop Agro, Inc.K043301GC TION GINGIVAL PROTECTORGC America, Inc.K040797BRITESMILE MASKING CREAMBritesmile, Inc.K022522PULPDENT PUTTY DAMPulpdent Corporation

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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