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FDA 510(k)

180 TIP, 1/A HANDPIECE .3MM END OPENING FOR OPHT.

K-Number: K920582 · 1992-05-08

Decision Date1992-05-08
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

180 TIP, 1/A HANDPIECE .3MM END OPENING FOR OPHT. is the device name listed in this FDA 510(k) record. The listed applicant is Site Microsurgical Systems, Inc.. It received FDA 510(k) clearance on 1992-05-08 under 510(k) number K920582. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 180 TIP, 1/A HANDPIECE .3MM END OPENING FOR OPHT.?

180 TIP, 1/A HANDPIECE .3MM END OPENING FOR OPHT. is a medical device that received FDA 510(k) clearance on 1992-05-08. The listed applicant is Site Microsurgical Systems, Inc.. The 510(k) number is K920582.

When did 180 TIP, 1/A HANDPIECE .3MM END OPENING FOR OPHT. receive FDA 510(k) clearance?

180 TIP, 1/A HANDPIECE .3MM END OPENING FOR OPHT. received FDA 510(k) clearance on 1992-05-08, under 510(k) number K920582.

Who is the listed applicant for 180 TIP, 1/A HANDPIECE .3MM END OPENING FOR OPHT.?

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

What is the FDA product code for 180 TIP, 1/A HANDPIECE .3MM END OPENING FOR OPHT.?

The FDA product code for 180 TIP, 1/A HANDPIECE .3MM END OPENING FOR OPHT. is HQE.

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 Site Microsurgical Systems, 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.

View all 30 devices →

Related Devices (Code: HQE)

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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