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FDA 510(k)

INFILTRATION PUMP SYRINGE

K-Number: K894882 · 1989-11-30

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

Device Summary

INFILTRATION PUMP SYRINGE 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 K894882. 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 INFILTRATION PUMP SYRINGE?

INFILTRATION PUMP SYRINGE 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 K894882.

When did INFILTRATION PUMP SYRINGE receive FDA 510(k) clearance?

INFILTRATION PUMP SYRINGE received FDA 510(k) clearance on 1989-11-30, under 510(k) number K894882.

Who is the listed applicant for INFILTRATION PUMP SYRINGE?

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 INFILTRATION PUMP SYRINGE?

The FDA product code for INFILTRATION PUMP SYRINGE 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 STEEK89488120GA X 7-1/2 THREADING BULLET POINT NEEDLEK89488016GA X 14 FOURTEEN LONG LONG BULLET POINT NEEDLK89487916GA X 10 MIDDLE SIZE BULLET POINT NEEDLEK89487316 GA X 10 BULLET POINT NEEDLEK89487520GA X 7-1/2 THREADING BULLET POINT NEEDLE

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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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