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FDA 510(k)

DENTAL AIR BRUSH

K-Number: K780460 · 1978-06-28

ApplicantM. Joel Gebhart, D.D.S.
Decision Date1978-06-28
Product CodeKOH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DENTAL AIR BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is M. Joel Gebhart, D.D.S.. It received FDA 510(k) clearance on 1978-06-28 under 510(k) number K780460. The device is classified under product code KOH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL AIR BRUSH?

DENTAL AIR BRUSH is a medical device that received FDA 510(k) clearance on 1978-06-28. The listed applicant is M. Joel Gebhart, D.D.S.. The 510(k) number is K780460.

When did DENTAL AIR BRUSH receive FDA 510(k) clearance?

DENTAL AIR BRUSH received FDA 510(k) clearance on 1978-06-28, under 510(k) number K780460.

Who is the listed applicant for DENTAL AIR BRUSH?

The FDA 510(k) record lists M. Joel Gebhart, D.D.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DENTAL AIR BRUSH?

The FDA product code for DENTAL AIR BRUSH is KOH.

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Related Devices (Code: KOH)

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.

K000212KSEA CHARDONNES MORCELLATION KNIFEKARL STORZ Endoscopy-America, Inc.K921730C-SECTION PACKMedikmark, Inc.K921732MINOR LAP SETMedikmark, Inc.K892693VAGINAL SPECULA: CUSCO, GUTTMAN, INFANTZinnanti Surgical Instruments, Inc.K891351NEWPORT LATERAL VAGINAL RETRACTORSimpson/Basye, Inc.K891035NEEDLE EXTENSIONSZinnanti Surgical Instruments, 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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