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FDA 510(k)

MICROSURGICAL INSTRUMENTS

K-Number: K874950 · 1987-12-30

ApplicantSolway, Inc.
Decision Date1987-12-30
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICROSURGICAL INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Solway, Inc.. It received FDA 510(k) clearance on 1987-12-30 under 510(k) number K874950. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSURGICAL INSTRUMENTS?

MICROSURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1987-12-30. The listed applicant is Solway, Inc.. The 510(k) number is K874950.

When did MICROSURGICAL INSTRUMENTS receive FDA 510(k) clearance?

MICROSURGICAL INSTRUMENTS received FDA 510(k) clearance on 1987-12-30, under 510(k) number K874950.

Who is the listed applicant for MICROSURGICAL INSTRUMENTS?

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

What is the FDA product code for MICROSURGICAL INSTRUMENTS?

The FDA product code for MICROSURGICAL INSTRUMENTS is HTD.

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 Solway, 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 13 devices →

Related Devices (Code: HTD)

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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