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FDA 510(k)

PUMP-JECT SYRINGE WITH LUER-LOCK

K-Number: K894041 · 1989-08-28

ApplicantZiehm International, Inc.
Decision Date1989-08-28
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PUMP-JECT SYRINGE WITH LUER-LOCK is the device name listed in this FDA 510(k) record. The listed applicant is Ziehm International, Inc.. It received FDA 510(k) clearance on 1989-08-28 under 510(k) number K894041. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PUMP-JECT SYRINGE WITH LUER-LOCK?

PUMP-JECT SYRINGE WITH LUER-LOCK is a medical device that received FDA 510(k) clearance on 1989-08-28. The listed applicant is Ziehm International, Inc.. The 510(k) number is K894041.

When did PUMP-JECT SYRINGE WITH LUER-LOCK receive FDA 510(k) clearance?

PUMP-JECT SYRINGE WITH LUER-LOCK received FDA 510(k) clearance on 1989-08-28, under 510(k) number K894041.

Who is the listed applicant for PUMP-JECT SYRINGE WITH LUER-LOCK?

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

What is the FDA product code for PUMP-JECT SYRINGE WITH LUER-LOCK?

The FDA product code for PUMP-JECT SYRINGE WITH LUER-LOCK is FRN.

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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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