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FDA 510(k)

ASTRON AIR POWERED HIGH SPEED DE PIECE

K-Number: K801684 · 1980-08-04

ApplicantPacific Dental Corp.
Decision Date1980-08-04
Product Code
DecisionSubstantially Equivalent

Device Summary

ASTRON AIR POWERED HIGH SPEED DE PIECE is the device name listed in this FDA 510(k) record. The listed applicant is Pacific Dental Corp.. It received FDA 510(k) clearance on 1980-08-04 under 510(k) number K801684. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASTRON AIR POWERED HIGH SPEED DE PIECE?

ASTRON AIR POWERED HIGH SPEED DE PIECE is a medical device that received FDA 510(k) clearance on 1980-08-04. The listed applicant is Pacific Dental Corp.. The 510(k) number is K801684.

When did ASTRON AIR POWERED HIGH SPEED DE PIECE receive FDA 510(k) clearance?

ASTRON AIR POWERED HIGH SPEED DE PIECE received FDA 510(k) clearance on 1980-08-04, under 510(k) number K801684.

Who is the listed applicant for ASTRON AIR POWERED HIGH SPEED DE PIECE?

The FDA 510(k) record lists Pacific Dental Corp. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Pacific Dental Corp. as applicant

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.

K821782BEACH ANESTHETIC SYRINGE CARTR. TYPEK821779BEACH AMALGAM CARRIER, GUN TYPEK821789BEACH CURETTE NO. 2 AND NO. 3 T.G.K821777BEACH MOUTH MIRRORK821778BEACH DRESSING PLIERK821780BEACH EXPLORER NO. 23T.G.

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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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