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FDA 510(k)

MASTERSCALE II

K-Number: K791704 · 1979-10-26

ApplicantLitton Dental Products
Decision Date1979-10-26
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MASTERSCALE II is the device name listed in this FDA 510(k) record. The listed applicant is Litton Dental Products. It received FDA 510(k) clearance on 1979-10-26 under 510(k) number K791704. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASTERSCALE II?

MASTERSCALE II is a medical device that received FDA 510(k) clearance on 1979-10-26. The listed applicant is Litton Dental Products. The 510(k) number is K791704.

When did MASTERSCALE II receive FDA 510(k) clearance?

MASTERSCALE II received FDA 510(k) clearance on 1979-10-26, under 510(k) number K791704.

Who is the listed applicant for MASTERSCALE II?

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

What is the FDA product code for MASTERSCALE II?

The FDA product code for MASTERSCALE II is ELC.

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Other records listing Litton Dental Products 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.

K791024ULTRASONIC DENTAL PROPHYLAXIS UNITK781114ULTRAMATE 990K781044ULTRASONIC DENTAL PROPHYLAXIS UNIT,SSMK772244ILLUMINATED DENTAL HANDPIECEK771556EXRK771557ULTRASON 990

View all 12 devices →

Related Devices (Code: ELC)

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.

K260773Varios Combi Pro2Nakanishi, Inc.K253254GBT Machine Airflow Prophylaxis MasterE.M.S Electro Medical Systems S.AK251689VARIOS 170 LUX SCALER SYSTEM (VA170LUXS10); VARIOS 170 LUX SCALER SYSTEM (VA170LUXS11); VARIOS 170 SCALER SYSTEM (VA170S11)Nakanishi, Inc.K242317Integrated Endo System (Meet Endo-II)Denjoy Dental Co., Ltd.K233844OdneCleanOdne AGK240707Ultrasonic Scaler (WD-JY-B002,WD-JY-W001,WD-JY-R003,WD-JY-G004,WD-JY-B003,WD-JY-C006,WD-JY-M0014, WD-JY-N0015,WD-JY-N0016,WD-JY-N0017,WD-JY-E007, WD-JY-F008,WD-JY-A005,WD-JY-H009,WD-JY-I0011, WD-JY-K0012,WD-JY-K0013,WD-JY-K0014, WD-JY-L0013,WD-JY-L0014,WD-JY-L0015, WD-JY-L0016,WD-JY-L0017)Shenzhen Micro Electric Intelligence Co., Ltd.

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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