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FDA 510(k)

ANESTHESIA CONDUCTION NEEDLE

K-Number: K962886 · 1996-10-09

ApplicantIspg, Inc.
Decision Date1996-10-09
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA CONDUCTION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Ispg, Inc.. It received FDA 510(k) clearance on 1996-10-09 under 510(k) number K962886. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANESTHESIA CONDUCTION NEEDLE?

ANESTHESIA CONDUCTION NEEDLE is a medical device that received FDA 510(k) clearance on 1996-10-09. The listed applicant is Ispg, Inc.. The 510(k) number is K962886.

When did ANESTHESIA CONDUCTION NEEDLE receive FDA 510(k) clearance?

ANESTHESIA CONDUCTION NEEDLE received FDA 510(k) clearance on 1996-10-09, under 510(k) number K962886.

Who is the listed applicant for ANESTHESIA CONDUCTION NEEDLE?

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

What is the FDA product code for ANESTHESIA CONDUCTION NEEDLE?

The FDA product code for ANESTHESIA CONDUCTION NEEDLE is BSP.

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.

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Other records listing Ispg, 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.

K012358CHIBA NEEDLEK962042GLASS SYRINGEK950133HYPODERMIC SYRINGE PISTON

Related Devices (Code: BSP)

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.

K243690SonoMSKPAJUNK GmbH MedizintechnologieK243682SonoPlex STIM; SonoPlex IIPAJUNK GmbH MedizintechnologieK250774SPROTTE® STANDARD (LUER/ NRFit®) Lumbar PuncturePAJUNK GmbH MedizintechnologieK243525SonoTAP and SonoTAP IIPAJUNK GmbH MedizintechnologieK241953SPROTTE® STANDARD (LUER/ NRFit®) AnesthesiologyPAJUNK GmbH MedizintechnologieK241954SonoBlock; SonoBlock IIPAJUNK GmbH Medizintechnologie

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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