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FDA 510(k)

SYRINGE DRIVER MS-16

K-Number: K830423 · 1983-03-07

ApplicantIntermedics, Inc.
Decision Date1983-03-07
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SYRINGE DRIVER MS-16 is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics, Inc.. It received FDA 510(k) clearance on 1983-03-07 under 510(k) number K830423. 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 SYRINGE DRIVER MS-16?

SYRINGE DRIVER MS-16 is a medical device that received FDA 510(k) clearance on 1983-03-07. The listed applicant is Intermedics, Inc.. The 510(k) number is K830423.

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

SYRINGE DRIVER MS-16 received FDA 510(k) clearance on 1983-03-07, under 510(k) number K830423.

Who is the listed applicant for SYRINGE DRIVER MS-16?

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

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

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

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Other records listing Intermedics, 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.

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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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