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FDA 510(k)

20GA X 7-1/2 THREADING BULLET POINT NEEDLE

K-Number: K894881 · 1989-11-30

ApplicantR. J. Doyle, Inc.
Decision Date1989-11-30
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

20GA X 7-1/2 THREADING BULLET POINT NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is R. J. Doyle, Inc.. It received FDA 510(k) clearance on 1989-11-30 under 510(k) number K894881. 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 20GA X 7-1/2 THREADING BULLET POINT NEEDLE?

20GA X 7-1/2 THREADING BULLET POINT NEEDLE is a medical device that received FDA 510(k) clearance on 1989-11-30. The listed applicant is R. J. Doyle, Inc.. The 510(k) number is K894881.

When did 20GA X 7-1/2 THREADING BULLET POINT NEEDLE receive FDA 510(k) clearance?

20GA X 7-1/2 THREADING BULLET POINT NEEDLE received FDA 510(k) clearance on 1989-11-30, under 510(k) number K894881.

Who is the listed applicant for 20GA X 7-1/2 THREADING BULLET POINT NEEDLE?

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

What is the FDA product code for 20GA X 7-1/2 THREADING BULLET POINT NEEDLE?

The FDA product code for 20GA X 7-1/2 THREADING BULLET POINT NEEDLE is BSP.

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Other records listing R. J. Doyle, 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.

K89487816GA X 6 BULLET POINT NEEDLE, FLEX STAINLESS STEEK89488016GA X 14 FOURTEEN LONG LONG BULLET POINT NEEDLK894882INFILTRATION PUMP SYRINGEK89487916GA X 10 MIDDLE SIZE BULLET POINT NEEDLEK89487316 GA X 10 BULLET POINT NEEDLEK89487520GA X 7-1/2 THREADING BULLET POINT NEEDLE

View all 10 devices →

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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