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FDA 510(k)

MS 16 SYRINGE DRIVER

K-Number: K802400 · 1980-12-16

ApplicantPrinceton Medical Instruments, Inc.
Decision Date1980-12-16
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MS 16 SYRINGE DRIVER is the device name listed in this FDA 510(k) record. The listed applicant is Princeton Medical Instruments, Inc.. It received FDA 510(k) clearance on 1980-12-16 under 510(k) number K802400. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MS 16 SYRINGE DRIVER?

MS 16 SYRINGE DRIVER is a medical device that received FDA 510(k) clearance on 1980-12-16. The listed applicant is Princeton Medical Instruments, Inc.. The 510(k) number is K802400.

When did MS 16 SYRINGE DRIVER receive FDA 510(k) clearance?

MS 16 SYRINGE DRIVER received FDA 510(k) clearance on 1980-12-16, under 510(k) number K802400.

Who is the listed applicant for MS 16 SYRINGE DRIVER?

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

What is the FDA product code for MS 16 SYRINGE DRIVER?

The FDA product code for MS 16 SYRINGE DRIVER is FRN.

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Other records listing Princeton Medical Instruments, 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.

K791729SYRINGE INFUSION PUMP

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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.

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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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