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FDA 510(k)

ADVANCE DISPOSABLE CONTROL SYRINGE

K-Number: K911732 · 1991-09-16

ApplicantAdvance Medical Designs, Inc.
Decision Date1991-09-16
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADVANCE DISPOSABLE 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 1991-09-16 under 510(k) number K911732. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANCE DISPOSABLE CONTROL SYRINGE?

ADVANCE DISPOSABLE CONTROL SYRINGE is a medical device that received FDA 510(k) clearance on 1991-09-16. The listed applicant is Advance Medical Designs, Inc.. The 510(k) number is K911732.

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

ADVANCE DISPOSABLE CONTROL SYRINGE received FDA 510(k) clearance on 1991-09-16, under 510(k) number K911732.

Who is the listed applicant for ADVANCE DISPOSABLE 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 ADVANCE DISPOSABLE CONTROL SYRINGE?

The FDA product code for ADVANCE DISPOSABLE CONTROL SYRINGE is IZI.

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Other records listing Advance Medical Designs, 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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Related Devices (Code: IZI)

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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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