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FDA 510(k)

IRRICLEAR EAR IRRIGATION SYRINGE

K-Number: K903759 · 1990-10-26

Decision Date1990-10-26
Product CodeKYZ
Advisory CommitteeHO
DecisionUnknown

Device Summary

IRRICLEAR EAR IRRIGATION SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Nortech Laboratories, Inc.. It received FDA 510(k) clearance on 1990-10-26 under 510(k) number K903759. The device is classified under product code KYZ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the IRRICLEAR EAR IRRIGATION SYRINGE?

IRRICLEAR EAR IRRIGATION SYRINGE is a medical device that received FDA 510(k) clearance on 1990-10-26. The listed applicant is Nortech Laboratories, Inc.. The 510(k) number is K903759.

When did IRRICLEAR EAR IRRIGATION SYRINGE receive FDA 510(k) clearance?

IRRICLEAR EAR IRRIGATION SYRINGE received FDA 510(k) clearance on 1990-10-26, under 510(k) number K903759.

Who is the listed applicant for IRRICLEAR EAR IRRIGATION SYRINGE?

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

What is the FDA product code for IRRICLEAR EAR IRRIGATION SYRINGE?

The FDA product code for IRRICLEAR EAR IRRIGATION SYRINGE is KYZ.

Related Clinical Trials

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.

Related Devices (Code: KYZ)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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