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FDA 510(k)

MEDICAL TECHNICAL PRODUCTS STANDARD ULTRASONIC HANDPIECE

K-Number: K940088 · 1994-08-04

Decision Date1994-08-04
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MEDICAL TECHNICAL PRODUCTS STANDARD ULTRASONIC HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Technical Products. It received FDA 510(k) clearance on 1994-08-04 under 510(k) number K940088. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICAL TECHNICAL PRODUCTS STANDARD ULTRASONIC HANDPIECE?

MEDICAL TECHNICAL PRODUCTS STANDARD ULTRASONIC HANDPIECE is a medical device that received FDA 510(k) clearance on 1994-08-04. The listed applicant is Medical Technical Products. The 510(k) number is K940088.

When did MEDICAL TECHNICAL PRODUCTS STANDARD ULTRASONIC HANDPIECE receive FDA 510(k) clearance?

MEDICAL TECHNICAL PRODUCTS STANDARD ULTRASONIC HANDPIECE received FDA 510(k) clearance on 1994-08-04, under 510(k) number K940088.

Who is the listed applicant for MEDICAL TECHNICAL PRODUCTS STANDARD ULTRASONIC HANDPIECE?

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

What is the FDA product code for MEDICAL TECHNICAL PRODUCTS STANDARD ULTRASONIC HANDPIECE?

The FDA product code for MEDICAL TECHNICAL PRODUCTS STANDARD ULTRASONIC HANDPIECE is HQC.

Related Clinical Trials

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.

Other records listing Medical Technical 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.

View all 8 devices →

Related Devices (Code: HQC)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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