FDA 510(k)

MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI)

K-Number: K864307 · 1986-11-18

Decision Date1986-11-18

Product CodeEIC

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI) is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 1986-11-18 under 510(k) number K864307. The device is classified under product code EIC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI)?

MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI) is a medical device that received FDA 510(k) clearance on 1986-11-18. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K864307.

When did MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI) receive FDA 510(k) clearance?

MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI) received FDA 510(k) clearance on 1986-11-18, under 510(k) number K864307.

Who is the listed applicant for MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI)?

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

What is the FDA product code for MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI)?

The FDA product code for MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI) is EIC.

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Related Devices (Code: EIC)

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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.