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FDA 510(k)

FOGCUTTER DENTAL MOUTH MIRROR

K-Number: K833310 · 1984-05-07

ApplicantHti, Inc.
Decision Date1984-05-07
Product CodeEAX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FOGCUTTER DENTAL MOUTH MIRROR is the device name listed in this FDA 510(k) record. The listed applicant is Hti, Inc.. It received FDA 510(k) clearance on 1984-05-07 under 510(k) number K833310. The device is classified under product code EAX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOGCUTTER DENTAL MOUTH MIRROR?

FOGCUTTER DENTAL MOUTH MIRROR is a medical device that received FDA 510(k) clearance on 1984-05-07. The listed applicant is Hti, Inc.. The 510(k) number is K833310.

When did FOGCUTTER DENTAL MOUTH MIRROR receive FDA 510(k) clearance?

FOGCUTTER DENTAL MOUTH MIRROR received FDA 510(k) clearance on 1984-05-07, under 510(k) number K833310.

Who is the listed applicant for FOGCUTTER DENTAL MOUTH MIRROR?

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

What is the FDA product code for FOGCUTTER DENTAL MOUTH MIRROR?

The FDA product code for FOGCUTTER DENTAL MOUTH MIRROR is EAX.

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Related Devices (Code: EAX)

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.

K946073ORALVUE DENTAL MIRRORHines Group , Ltd.K935906RANIR PLAX RXRanir/Dcp Corp.K941574RETRO MIRRORUnion Broach, Div. Moyco Industries, Inc.K935687NILDentalsafe Systems Pty., Ltd.K863767GLASS MOUTH MIRRORS, REUSABLEThe Medical Group, Inc.K863766DISPOSABLE MOUTH MIRRORS, SINGLE USE ONLYThe Medical Group, Inc.

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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