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FDA 510(k)

SENSI-TOUCH EPIDURAL ANESTHESIA FILTER

K-Number: K954525 · 1996-01-19

ApplicantSherwood Medical Co.
Decision Date1996-01-19
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SENSI-TOUCH EPIDURAL ANESTHESIA FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1996-01-19 under 510(k) number K954525. The device is classified under product code BXN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENSI-TOUCH EPIDURAL ANESTHESIA FILTER?

SENSI-TOUCH EPIDURAL ANESTHESIA FILTER is a medical device that received FDA 510(k) clearance on 1996-01-19. The listed applicant is Sherwood Medical Co.. The 510(k) number is K954525.

When did SENSI-TOUCH EPIDURAL ANESTHESIA FILTER receive FDA 510(k) clearance?

SENSI-TOUCH EPIDURAL ANESTHESIA FILTER received FDA 510(k) clearance on 1996-01-19, under 510(k) number K954525.

Who is the listed applicant for SENSI-TOUCH EPIDURAL ANESTHESIA FILTER?

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

What is the FDA product code for SENSI-TOUCH EPIDURAL ANESTHESIA FILTER?

The FDA product code for SENSI-TOUCH EPIDURAL ANESTHESIA FILTER is BXN.

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Other records listing Sherwood Medical Co. 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.

K981365MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONSK960982MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULAK962880SENSI-TOUCH COMBO SPINAL/EPIDURAL REGIONAL ANESTHESIA DELIVERY SYSTEMK960574ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEMK960677KANGAROO JEJUNAL FEEDING SYSTEMK960632KANGAROO FEEDING TUBE PLACMENT STYLET

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Related Devices (Code: BXN)

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.

K213049STIMPOD NMS450 Nerve StimulatorXavant Technology (Pty), Ltd.K162086MultiStim ECOPAJUNK GmbH MedizintechnologieK153045SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve StimulatorEasy Med Instrument Co., Ltd.K121743EASYMED PERIPHERAL NERVE STIMULATOR-SUNSTINSunmed, LLCK111985MYOGUIDE SYSTEM MODEL 8008Intronix Technologies Corp.K110118STIMTRODE SINGLE USE NERVE STIMULATORXavant Technology (Pty), Ltd.

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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