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FDA 510(k)

MAX-I-PROBE ENDODONTIC SEALER DELIVERY SYSTEM

K-Number: K971622 · 1997-06-20

ApplicantMpl Technologies, Inc.
Decision Date1997-06-20
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MAX-I-PROBE ENDODONTIC SEALER DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Mpl Technologies, Inc.. It received FDA 510(k) clearance on 1997-06-20 under 510(k) number K971622. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAX-I-PROBE ENDODONTIC SEALER DELIVERY SYSTEM?

MAX-I-PROBE ENDODONTIC SEALER DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 1997-06-20. The listed applicant is Mpl Technologies, Inc.. The 510(k) number is K971622.

When did MAX-I-PROBE ENDODONTIC SEALER DELIVERY SYSTEM receive FDA 510(k) clearance?

MAX-I-PROBE ENDODONTIC SEALER DELIVERY SYSTEM received FDA 510(k) clearance on 1997-06-20, under 510(k) number K971622.

Who is the listed applicant for MAX-I-PROBE ENDODONTIC SEALER DELIVERY SYSTEM?

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

What is the FDA product code for MAX-I-PROBE ENDODONTIC SEALER DELIVERY SYSTEM?

The FDA product code for MAX-I-PROBE ENDODONTIC SEALER DELIVERY SYSTEM is KIF.

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Related Devices (Code: KIF)

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.

K262050Vioseal XSpident Co., Ltd.K253909NeoPEX™ Pre-Mixed Obturation PasteNuSmile, Ltd.K261514Calcium Hydroxide Temporary Filling Material (KP-Cal)Guilin Kevin Peter Technology Co., Ltd.K261415Injectable Root Canal Sealer (KP-Root SP)Guilin Kevin Peter Technology Co., Ltd.K253167Any-PasteMediclus Co., Ltd.K252890ZenSeal ProKerr Corporation

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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