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FDA 510(k)

ULTRASONIC TOOTH SCALER MODEL DSCIOP

K-Number: K852540 · 1985-07-01

ApplicantParkell, Inc.
Decision Date1985-07-01
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ULTRASONIC TOOTH SCALER MODEL DSCIOP is the device name listed in this FDA 510(k) record. The listed applicant is Parkell, Inc.. It received FDA 510(k) clearance on 1985-07-01 under 510(k) number K852540. 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 ULTRASONIC TOOTH SCALER MODEL DSCIOP?

ULTRASONIC TOOTH SCALER MODEL DSCIOP is a medical device that received FDA 510(k) clearance on 1985-07-01. The listed applicant is Parkell, Inc.. The 510(k) number is K852540.

When did ULTRASONIC TOOTH SCALER MODEL DSCIOP receive FDA 510(k) clearance?

ULTRASONIC TOOTH SCALER MODEL DSCIOP received FDA 510(k) clearance on 1985-07-01, under 510(k) number K852540.

Who is the listed applicant for ULTRASONIC TOOTH SCALER MODEL DSCIOP?

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

What is the FDA product code for ULTRASONIC TOOTH SCALER MODEL DSCIOP?

The FDA product code for ULTRASONIC TOOTH SCALER MODEL DSCIOP is ELC.

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Other records listing Parkell, Inc. as applicant

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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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