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FDA 510(k)

RUBBER DAM CLAMP

K-Number: K923163 · 1992-12-28

ApplicantAseptico, Inc.
Decision Date1992-12-28
Product CodeEIE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RUBBER DAM CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Aseptico, Inc.. It received FDA 510(k) clearance on 1992-12-28 under 510(k) number K923163. 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 RUBBER DAM CLAMP?

RUBBER DAM CLAMP is a medical device that received FDA 510(k) clearance on 1992-12-28. The listed applicant is Aseptico, Inc.. The 510(k) number is K923163.

When did RUBBER DAM CLAMP receive FDA 510(k) clearance?

RUBBER DAM CLAMP received FDA 510(k) clearance on 1992-12-28, under 510(k) number K923163.

Who is the listed applicant for RUBBER DAM CLAMP?

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

What is the FDA product code for RUBBER DAM CLAMP?

The FDA product code for RUBBER DAM CLAMP is EIE.

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Other records listing Aseptico, Inc. as applicant

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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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