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FDA 510(k)

PHARMASEAL CLEAR HUB SPINAL NEEDLE

K-Number: K920305 · 1993-01-27

ApplicantBaxter Healthcare Corp
Decision Date1993-01-27
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PHARMASEAL CLEAR HUB SPINAL NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1993-01-27 under 510(k) number K920305. 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 PHARMASEAL CLEAR HUB SPINAL NEEDLE?

PHARMASEAL CLEAR HUB SPINAL NEEDLE is a medical device that received FDA 510(k) clearance on 1993-01-27. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K920305.

When did PHARMASEAL CLEAR HUB SPINAL NEEDLE receive FDA 510(k) clearance?

PHARMASEAL CLEAR HUB SPINAL NEEDLE received FDA 510(k) clearance on 1993-01-27, under 510(k) number K920305.

Who is the listed applicant for PHARMASEAL CLEAR HUB SPINAL NEEDLE?

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

What is the FDA product code for PHARMASEAL CLEAR HUB SPINAL NEEDLE?

The FDA product code for PHARMASEAL CLEAR HUB SPINAL NEEDLE is BSP.

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Other records listing Baxter Healthcare Corp as applicant

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K190910PrisMax System Version 2K163530PrisMax Control UnitK132734NEUTRAL LUER ACTIVATED DEVICE (ONE-LINK NEEDLE-FREE IV CONNECTOR) AND EXTENSION SETSK130245LARGE BORE STOPCOCK WITH ROTATING MALE LUER LOCK/LARGE BORE STOPCOCK WITH EXTENSION SET, GANG LARGE BORE STOPCOCK MANIFOK123874INTERLINK SYSTEM BURETROL SOLUTION SETS, INTERLINK SYSTEM BURETROL SOLUTION SETS, CONTINUED, CLEARLINK SYSTEM BURETROL SK123868INTERLINK SYSTEM LEVER LOCK CANNULA WITH CHECK VALVE, SECONDARY MEDICATION SETS, SOLUTION SETS, CONTINU-FLO SOLUTION SET

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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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