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FDA 510(k)

DENTAL 911

K-Number: K941066 · 1995-05-24

ApplicantL.A.F. Industries, Inc.
Decision Date1995-05-24
Product CodeEMB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL 911 is the device name listed in this FDA 510(k) record. The listed applicant is L.A.F. Industries, Inc.. It received FDA 510(k) clearance on 1995-05-24 under 510(k) number K941066. The device is classified under product code EMB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL 911?

DENTAL 911 is a medical device that received FDA 510(k) clearance on 1995-05-24. The listed applicant is L.A.F. Industries, Inc.. The 510(k) number is K941066.

When did DENTAL 911 receive FDA 510(k) clearance?

DENTAL 911 received FDA 510(k) clearance on 1995-05-24, under 510(k) number K941066.

Who is the listed applicant for DENTAL 911?

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

What is the FDA product code for DENTAL 911?

The FDA product code for DENTAL 911 is EMB.

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Related Devices (Code: EMB)

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.

K161630Provicol QM PlusVoco GmbHK120695DENTIST IN A BOX DENTAL EMERGENCY KIT PLUS TOOTH TRAUMA CARE KITDentist IN A Box Pty., Ltd.K110759TEMPOCEMDmg USA, Inc.K073539PROVISA CEMCavex Holland BVK020158NON-EUGENOL TEMPORARY CEMENTJ. Morita USA, Inc.K861681DENTIMEDIC DENTAL EMERGENCY KITDentimedic

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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