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FDA 510(k)

MPI MON-IT II, SMART SAFETY SYSTEM

K-Number: K821169 · 1982-08-06

ApplicantMedical Plastics, Inc.
Decision Date1982-08-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MPI MON-IT II, SMART SAFETY SYSTEM 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 1982-08-06 under 510(k) number K821169. 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 MON-IT II, SMART SAFETY SYSTEM?

MPI MON-IT II, SMART SAFETY SYSTEM is a medical device that received FDA 510(k) clearance on 1982-08-06. The listed applicant is Medical Plastics, Inc.. The 510(k) number is K821169.

When did MPI MON-IT II, SMART SAFETY SYSTEM receive FDA 510(k) clearance?

MPI MON-IT II, SMART SAFETY SYSTEM received FDA 510(k) clearance on 1982-08-06, under 510(k) number K821169.

Who is the listed applicant for MPI MON-IT II, SMART SAFETY SYSTEM?

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 MON-IT II, SMART SAFETY SYSTEM?

The FDA product code for MPI MON-IT II, SMART SAFETY SYSTEM 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 DRAPEK822072MPI ELECTROSURGICAL CAPACTIVE DISPERK781148ELECTROSURGICAL PENCIL SYSTEM

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Related Devices (Code: GEI)

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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.

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