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FDA 510(k)

TSK STERIJECT STERILE EPIDURAL NEEDLE

K-Number: K854149 · 1985-10-23

ApplicantPharmacia, Inc.
Decision Date1985-10-23
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TSK STERIJECT STERILE EPIDURAL NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia, Inc.. It received FDA 510(k) clearance on 1985-10-23 under 510(k) number K854149. 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 TSK STERIJECT STERILE EPIDURAL NEEDLE?

TSK STERIJECT STERILE EPIDURAL NEEDLE is a medical device that received FDA 510(k) clearance on 1985-10-23. The listed applicant is Pharmacia, Inc.. The 510(k) number is K854149.

When did TSK STERIJECT STERILE EPIDURAL NEEDLE receive FDA 510(k) clearance?

TSK STERIJECT STERILE EPIDURAL NEEDLE received FDA 510(k) clearance on 1985-10-23, under 510(k) number K854149.

Who is the listed applicant for TSK STERIJECT STERILE EPIDURAL NEEDLE?

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

What is the FDA product code for TSK STERIJECT STERILE EPIDURAL NEEDLE?

The FDA product code for TSK STERIJECT STERILE EPIDURAL NEEDLE is BSP.

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Other records listing Pharmacia, 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.

K974350ALLERGAN IMMUNO CAP M4, M8, K70K972364UNICAP PHADIATOPK972068UNICAP SPECIFIC IGE FEIA ASSAY, LATEX ALLERGEN IMMUNOCAP K82K970420MASTERCAP AM 5.0/MASTERCAP RM 5.0K964152UNICAP TOTAL IGE ASSAY/PHARMACIA TOTAL IGE CONTROLS LMHK962274UNICAP 100

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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

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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