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FDA 510(k)

9110 SYRINGE

K-Number: K822774 · 1982-11-03

ApplicantCardiac Pacemakers, Inc.
Decision Date1982-11-03
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

9110 SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Cardiac Pacemakers, Inc.. It received FDA 510(k) clearance on 1982-11-03 under 510(k) number K822774. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 9110 SYRINGE?

9110 SYRINGE is a medical device that received FDA 510(k) clearance on 1982-11-03. The listed applicant is Cardiac Pacemakers, Inc.. The 510(k) number is K822774.

When did 9110 SYRINGE receive FDA 510(k) clearance?

9110 SYRINGE received FDA 510(k) clearance on 1982-11-03, under 510(k) number K822774.

Who is the listed applicant for 9110 SYRINGE?

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

What is the FDA product code for 9110 SYRINGE?

The FDA product code for 9110 SYRINGE is FMF.

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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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