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FDA 510(k)

AIROTOS LF HANDPIECE

K-Number: K761275 · 1976-12-23

ApplicantDentsply Intl.
Decision Date1976-12-23
Product CodeDZA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AIROTOS LF HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1976-12-23 under 510(k) number K761275. The device is classified under product code DZA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIROTOS LF HANDPIECE?

AIROTOS LF HANDPIECE is a medical device that received FDA 510(k) clearance on 1976-12-23. The listed applicant is Dentsply Intl.. The 510(k) number is K761275.

When did AIROTOS LF HANDPIECE receive FDA 510(k) clearance?

AIROTOS LF HANDPIECE received FDA 510(k) clearance on 1976-12-23, under 510(k) number K761275.

Who is the listed applicant for AIROTOS LF HANDPIECE?

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

What is the FDA product code for AIROTOS LF HANDPIECE?

The FDA product code for AIROTOS LF HANDPIECE is DZA.

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Other records listing Dentsply Intl. 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.

K123615IRIS - HIGH STRENGTH GLASS CERAMICK072730FRIADENT CERCON AND ANKYLOS CERCON BALANCE ABUTMENTSK070538XP BOND DUAL CURE UNIVERSAL TOTAL ETCH ADHESIVEK070019CARRARA VOLUMIAK061427PRE-IMPRESSION CONDITIONING SOLUTIONK052334CAVITRON RF ULTRASONIC SCALER SYSTEM WITH STERIMATE HANDPIECE, MODEL G-131

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Related Devices (Code: DZA)

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.

K984508SURGICAL CONTRA-ANGLE HANDPIECES, MODELS 975 AE,979 E/KM, 985 AE, 986 AE, 988 E/KM AND SURGICAL STRAIGHT HANDPIECES MODW&H Dentalwerk Buermoos GmbHK962979S-53 INTRORAL DENTAL SYSTEMDel Medical Systems Corp.K954790PROFILE NICKEL TITANIUM ROTARY INSTRUMENTSTulsa Dental Products, Ltd.K914724ADA SHANK EXTENSIONImplant Corp. of AmericaK905418GATES GLIDDEN DRILLSThe Hygenic Corp.K901097FILLOCK REAMERIvoclar North America, 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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