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FDA 510(k)

PROPAK

K-Number: K924118 · 1993-07-13

ApplicantDental Services, Inc.
Decision Date1993-07-13
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROPAK is the device name listed in this FDA 510(k) record. The listed applicant is Dental Services, Inc.. It received FDA 510(k) clearance on 1993-07-13 under 510(k) number K924118. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROPAK?

PROPAK is a medical device that received FDA 510(k) clearance on 1993-07-13. The listed applicant is Dental Services, Inc.. The 510(k) number is K924118.

When did PROPAK receive FDA 510(k) clearance?

PROPAK received FDA 510(k) clearance on 1993-07-13, under 510(k) number K924118.

Who is the listed applicant for PROPAK?

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

What is the FDA product code for PROPAK?

The FDA product code for PROPAK is KCT.

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Related Devices (Code: KCT)

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.

K253988LiteSet TraysNobel Biocare ABK261935Surgical and Prosthetic TraysDentsply Sirona, Inc.K253187SteriBest® Sterilization Tray SystemMastel SurgicalK260726Straumann® ProClean™ Cassette (041.800 ; 041.801)Institut Straumann AGK252854SteriTite Container System with MediTray ProductsCase Medical, Inc.K253791PUREVUE™ Quick Connect Cannula System Tray; PUREVUE™ Quick Connect Cannula System LidDePuy Mitek, Inc.

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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