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FDA 510(k)

DISPOSABLE CORONARY CONTROL SYRINGE

K-Number: K902346 · 1990-06-26

ApplicantAdvance Medical Designs, Inc.
Decision Date1990-06-26
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE CORONARY CONTROL SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Advance Medical Designs, Inc.. It received FDA 510(k) clearance on 1990-06-26 under 510(k) number K902346. 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 DISPOSABLE CORONARY CONTROL SYRINGE?

DISPOSABLE CORONARY CONTROL SYRINGE is a medical device that received FDA 510(k) clearance on 1990-06-26. The listed applicant is Advance Medical Designs, Inc.. The 510(k) number is K902346.

When did DISPOSABLE CORONARY CONTROL SYRINGE receive FDA 510(k) clearance?

DISPOSABLE CORONARY CONTROL SYRINGE received FDA 510(k) clearance on 1990-06-26, under 510(k) number K902346.

Who is the listed applicant for DISPOSABLE CORONARY CONTROL SYRINGE?

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

What is the FDA product code for DISPOSABLE CORONARY CONTROL SYRINGE?

The FDA product code for DISPOSABLE CORONARY CONTROL SYRINGE is FMF.

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Other records listing Advance Medical Designs, Inc. as applicant

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Related Devices (Code: 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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