Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS

K-Number: K874962 · 1988-02-02

ApplicantSolway, Inc.
Decision Date1988-02-02
Product CodeHAO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS is the device name listed in this FDA 510(k) record. The listed applicant is Solway, Inc.. It received FDA 510(k) clearance on 1988-02-02 under 510(k) number K874962. The device is classified under product code HAO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS?

FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS is a medical device that received FDA 510(k) clearance on 1988-02-02. The listed applicant is Solway, Inc.. The 510(k) number is K874962.

When did FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS receive FDA 510(k) clearance?

FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS received FDA 510(k) clearance on 1988-02-02, under 510(k) number K874962.

Who is the listed applicant for FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS?

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 FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS?

The FDA product code for FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS is HAO.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 INSTRUMENTSK874956SELF-RETAINING RETRACTOR FOR NEUROSURGERYK874964DENTAL HAND INSTRUMENTSK875043RONGEUR (NEUROSURGICAL INSTRUMENTS)K874966TUNING FORKSK874959VASCULAR CLAMP

View all 13 devices →

Related Devices (Code: HAO)

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.

K220920Matreneu Percutaneous Balloon Compression KitShenzhen Shineyard Medical Device Co. , Ltd.K940973MULLAN GANGLION MICROCOMPRESSION SETCook, Inc.K951492RIB RESECTORUnited States Surgical, A Division of Tyco HealthcK943115AUTO SUTURE PITUITARY SPINAL RONGEURUnited States Surgical, A Division of Tyco HealthcK942968AUTO SUTURE SPINAL OSTEOTOMEUnited States Surgical, A Division of Tyco HealthcK942969AUTO SUTURE SPINAL NERVE HOOKUnited States Surgical, A Division of Tyco Healthc

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.

↑