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FDA 510(k)

VERRES NEEDLE

K-Number: K942484 · 1994-06-24

ApplicantLinvatec Corp.
Decision Date1994-06-24
Product CodeFHO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VERRES NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Linvatec Corp.. It received FDA 510(k) clearance on 1994-06-24 under 510(k) number K942484. The device is classified under product code FHO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERRES NEEDLE?

VERRES NEEDLE is a medical device that received FDA 510(k) clearance on 1994-06-24. The listed applicant is Linvatec Corp.. The 510(k) number is K942484.

When did VERRES NEEDLE receive FDA 510(k) clearance?

VERRES NEEDLE received FDA 510(k) clearance on 1994-06-24, under 510(k) number K942484.

Who is the listed applicant for VERRES NEEDLE?

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

What is the FDA product code for VERRES NEEDLE?

The FDA product code for VERRES NEEDLE is FHO.

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Other records listing Linvatec Corp. as applicant

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Related Devices (Code: FHO)

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.

K172120Veress NeedleWickimed (Huizhou) Medical Equipment Manufacturing Co.,LtdK121370VECTEC DISPOSABLE PNEUMOPERITONEUM NEEDLEVectecK010779MODIFICATION TO:LAPAROSCOPIC/ENDOSCOPIC INSTRUMENTGibbons Surgical Corp.K970788PNEUMO-MATIC INSUFFLATION NEEDLEApple Medical Corp.K960574ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEMSherwood Medical Co.K951894ACCESS EXPANSION SYSTEMMicro-Medical Devices, 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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