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FDA 510(k)

EM 1149 OPTIMIZE SCOTCHPLATE CONDUC ADHES DISP ELE

K-Number: K900332 · 1990-02-13

Applicant3M Company
Decision Date1990-02-13
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EM 1149 OPTIMIZE SCOTCHPLATE CONDUC ADHES DISP ELE is the device name listed in this FDA 510(k) record. The listed applicant is 3M Company. It received FDA 510(k) clearance on 1990-02-13 under 510(k) number K900332. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EM 1149 OPTIMIZE SCOTCHPLATE CONDUC ADHES DISP ELE?

EM 1149 OPTIMIZE SCOTCHPLATE CONDUC ADHES DISP ELE is a medical device that received FDA 510(k) clearance on 1990-02-13. The listed applicant is 3M Company. The 510(k) number is K900332.

When did EM 1149 OPTIMIZE SCOTCHPLATE CONDUC ADHES DISP ELE receive FDA 510(k) clearance?

EM 1149 OPTIMIZE SCOTCHPLATE CONDUC ADHES DISP ELE received FDA 510(k) clearance on 1990-02-13, under 510(k) number K900332.

Who is the listed applicant for EM 1149 OPTIMIZE SCOTCHPLATE CONDUC ADHES DISP ELE?

The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EM 1149 OPTIMIZE SCOTCHPLATE CONDUC ADHES DISP ELE?

The FDA product code for EM 1149 OPTIMIZE SCOTCHPLATE CONDUC ADHES DISP ELE is GEI.

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Other records listing 3M Company as applicant

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Related Devices (Code: GEI)

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K261959Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)Stryker InstrumentsK254196HARMONIC 1100 Shears (HAR1120); HARMONIC 1100 Shears (HAR1136)Ethicon Endo-Surgery, LLCK261070LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coatedCovidien, LLCK254185Potenza PrimeJeisys Medical IncorporatedK262364Ellian Enigma RF DeviceEllian CorpK253859Scarlet Pro (Scarlet Pro)VIOL Co., Ltd.

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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