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FDA 510(k)

MPI ELECTROSURGICAL CAPACTIVE DISPER

K-Number: K822072 · 1982-08-19

ApplicantMedical Plastics, Inc.
Decision Date1982-08-19
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MPI ELECTROSURGICAL CAPACTIVE DISPER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Plastics, Inc.. It received FDA 510(k) clearance on 1982-08-19 under 510(k) number K822072. 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 MPI ELECTROSURGICAL CAPACTIVE DISPER?

MPI ELECTROSURGICAL CAPACTIVE DISPER is a medical device that received FDA 510(k) clearance on 1982-08-19. The listed applicant is Medical Plastics, Inc.. The 510(k) number is K822072.

When did MPI ELECTROSURGICAL CAPACTIVE DISPER receive FDA 510(k) clearance?

MPI ELECTROSURGICAL CAPACTIVE DISPER received FDA 510(k) clearance on 1982-08-19, under 510(k) number K822072.

Who is the listed applicant for MPI ELECTROSURGICAL CAPACTIVE DISPER?

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

What is the FDA product code for MPI ELECTROSURGICAL CAPACTIVE DISPER?

The FDA product code for MPI ELECTROSURGICAL CAPACTIVE DISPER is GEI.

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Other records listing Medical Plastics, Inc. as applicant

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.

K902384ABDOMINAL OR C-SECTION DRAPE SHEETK896088FEMORAL ANGIOGRAPHY DRAPEK895404UNDER BUTTOCKS DRAPEK890101FEMORAL ANGIOGRAPHY DRAPEK821169MPI MON-IT II, SMART SAFETY SYSTEMK781148ELECTROSURGICAL PENCIL SYSTEM

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Related Devices (Code: GEI)

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.

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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