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FDA 510(k)

MAX-I-PROBE PERIODONTAL ENDODONTIC PROB

K-Number: K840237 · 1984-04-05

ApplicantSmith & Nephew, Mpl Division
Decision Date1984-04-05
Product CodeEIC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MAX-I-PROBE PERIODONTAL ENDODONTIC PROB is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Mpl Division. It received FDA 510(k) clearance on 1984-04-05 under 510(k) number K840237. 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 PERIODONTAL ENDODONTIC PROB?

MAX-I-PROBE PERIODONTAL ENDODONTIC PROB is a medical device that received FDA 510(k) clearance on 1984-04-05. The listed applicant is Smith & Nephew, Mpl Division. The 510(k) number is K840237.

When did MAX-I-PROBE PERIODONTAL ENDODONTIC PROB receive FDA 510(k) clearance?

MAX-I-PROBE PERIODONTAL ENDODONTIC PROB received FDA 510(k) clearance on 1984-04-05, under 510(k) number K840237.

Who is the listed applicant for MAX-I-PROBE PERIODONTAL ENDODONTIC PROB?

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

What is the FDA product code for MAX-I-PROBE PERIODONTAL ENDODONTIC PROB?

The FDA product code for MAX-I-PROBE PERIODONTAL ENDODONTIC PROB is EIC.

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Other records listing Smith & Nephew, Mpl Division as applicant

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K843314MPL HYPO BRAND BREECH LOAD ASPIR SYRINGEK841280SOLOPAK BRAND FILTER NEEDLE W/5 MICROK833304HYPO BRAND DISPOS. DENTAL NEEDLES-PLASTK832126MICRO Z DISPOS. SPINAL ANESTH. NEEDLEK831765HERAPIN LOCK FLUSH SOLUTION USE KITK830524HENKE JECT PRESSURE SYRINGE

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Related Devices (Code: EIC)

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.

K972234RCT GEL ROOT CANAL THERAPY GELDentsply Intl.K864307MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI)Smith & Nephew, Inc.K861846HYDRON ROOT CANAL FILLING & MARK IV STARTER KITSolar Dental Co., Inc.K851944MAX-I-PROBE HANDPIECESolo Pak LaboratoriesK811889R & S SERIES FITTING TOOLSSuncoast Dental Corp.K811594WATER PISTOLAus-Tex Dental Mfg. & Design

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.

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