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FDA 510(k)

AIRES TUOHY NEEDLES 17GA. X 4 1/2

K-Number: K850111 · 1985-01-24

ApplicantAries Medical, Inc.
Decision Date1985-01-24
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AIRES TUOHY NEEDLES 17GA. X 4 1/2 is the device name listed in this FDA 510(k) record. The listed applicant is Aries Medical, Inc.. It received FDA 510(k) clearance on 1985-01-24 under 510(k) number K850111. 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 AIRES TUOHY NEEDLES 17GA. X 4 1/2?

AIRES TUOHY NEEDLES 17GA. X 4 1/2 is a medical device that received FDA 510(k) clearance on 1985-01-24. The listed applicant is Aries Medical, Inc.. The 510(k) number is K850111.

When did AIRES TUOHY NEEDLES 17GA. X 4 1/2 receive FDA 510(k) clearance?

AIRES TUOHY NEEDLES 17GA. X 4 1/2 received FDA 510(k) clearance on 1985-01-24, under 510(k) number K850111.

Who is the listed applicant for AIRES TUOHY NEEDLES 17GA. X 4 1/2?

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

What is the FDA product code for AIRES TUOHY NEEDLES 17GA. X 4 1/2?

The FDA product code for AIRES TUOHY NEEDLES 17GA. X 4 1/2 is BSP.

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Other records listing Aries Medical, Inc. as applicant

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K912604SJM/CAD ISOFLOW(TM) CENTRIFUGAL PUMP 2100CP, MODIFK903925ARIES MELDICAL MODEL 2100HC HANK CRANKK903442ARIES TAPERSEAL(TM) SHEATHK895433ARIES 30CC & 50CC INTRA-AORTIC BALLOON & CONT. SYSK882289ARIES 40CC PERCU. (D/L) INTRA-AORTIC BALLOON CATH.K86453740CC PERCUTANEOUS PRE-FURL (D/L) BALLOON CATHETER

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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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