FDA 510(k)

PRO-KUP

K-Number: K770556 · 1977-03-24

Decision Date1977-03-24

Product CodeEHK

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

PRO-KUP is the device name listed in this FDA 510(k) record. The listed applicant is Dental Control Products. It received FDA 510(k) clearance on 1977-03-24 under 510(k) number K770556. The device is classified under product code EHK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRO-KUP?

PRO-KUP is a medical device that received FDA 510(k) clearance on 1977-03-24. The listed applicant is Dental Control Products. The 510(k) number is K770556.

When did PRO-KUP receive FDA 510(k) clearance?

PRO-KUP received FDA 510(k) clearance on 1977-03-24, under 510(k) number K770556.

Who is the listed applicant for PRO-KUP?

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

What is the FDA product code for PRO-KUP?

The FDA product code for PRO-KUP is EHK.

Related Devices (Code: EHK)

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.

K953628PROPHY ANGLERolence Enterprise Co. , Ltd.K951016DISPOSABLE PROPHYLAXIS ANGLEPreventive Technologies, Inc.K900507DISPOSABLE SCREW TYPE PROPHY BRUSHDentsply Intl.K864059DENTAL PROPHY CUPS (VARIOUS TYPES)Mission White Dental, Inc.K803155PROPHYLAXIS CUP.Teledyne Densco K790723PROPHYLAXIS CUPS AND POLISHERSYoung Dental Manufacturing Co. 1, LLC

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.