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FDA 510(k)

ASPIRATING AND IRRIGATING CYSTS NEEDLES

K-Number: K885283 · 1989-03-22

Decision Date1989-03-22
Product CodeGDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ASPIRATING AND IRRIGATING CYSTS NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Go Medical Industries Pty. , Ltd.. It received FDA 510(k) clearance on 1989-03-22 under 510(k) number K885283. The device is classified under product code GDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASPIRATING AND IRRIGATING CYSTS NEEDLES?

ASPIRATING AND IRRIGATING CYSTS NEEDLES is a medical device that received FDA 510(k) clearance on 1989-03-22. The listed applicant is Go Medical Industries Pty. , Ltd.. The 510(k) number is K885283.

When did ASPIRATING AND IRRIGATING CYSTS NEEDLES receive FDA 510(k) clearance?

ASPIRATING AND IRRIGATING CYSTS NEEDLES received FDA 510(k) clearance on 1989-03-22, under 510(k) number K885283.

Who is the listed applicant for ASPIRATING AND IRRIGATING CYSTS NEEDLES?

The FDA 510(k) record lists Go Medical Industries Pty. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ASPIRATING AND IRRIGATING CYSTS NEEDLES?

The FDA product code for ASPIRATING AND IRRIGATING CYSTS NEEDLES is GDM.

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.

Other records listing Go Medical Industries Pty. , Ltd. 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.

View all 11 devices →

Related Devices (Code: GDM)

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

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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