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FDA 510(k)

MANUAL SURGICAL INSTRUMENTS FOR GENERAL USE

K-Number: K874965 · 1987-12-30

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

Device Summary

MANUAL SURGICAL INSTRUMENTS FOR GENERAL USE 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 K874965. 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 MANUAL SURGICAL INSTRUMENTS FOR GENERAL USE?

MANUAL SURGICAL INSTRUMENTS FOR GENERAL USE 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 K874965.

When did MANUAL SURGICAL INSTRUMENTS FOR GENERAL USE receive FDA 510(k) clearance?

MANUAL SURGICAL INSTRUMENTS FOR GENERAL USE received FDA 510(k) clearance on 1987-12-30, under 510(k) number K874965.

Who is the listed applicant for MANUAL SURGICAL INSTRUMENTS FOR GENERAL USE?

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 MANUAL SURGICAL INSTRUMENTS FOR GENERAL USE?

The FDA product code for MANUAL SURGICAL INSTRUMENTS FOR GENERAL USE is HTD.

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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.

K874960CARDIOVASCULAR SURGICAL INSTRUMENTSK874962FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULASK874956SELF-RETAINING RETRACTOR FOR NEUROSURGERYK874964DENTAL HAND INSTRUMENTSK875043RONGEUR (NEUROSURGICAL INSTRUMENTS)K874966TUNING FORKS

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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.

K051281THE NEEDLE CATCHERE.D.Medical , Ltd.K974593SEMKIN INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K974594SEMKIN BIPOLAR FORCEPTitan Mfg., Inc.K974595CUSHING BAYONET, INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K913964MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPSMarlo Surgical TechnologyK911180CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPSNorthgate Technologies, Inc.

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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