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FDA 510(k)

IVAC(R) SYRINGE PUMP - MODEL 770

K-Number: K901550 · 1990-10-04

ApplicantY
Decision Date1990-10-04
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IVAC(R) SYRINGE PUMP - MODEL 770 is the device name listed in this FDA 510(k) record. The listed applicant is Y. It received FDA 510(k) clearance on 1990-10-04 under 510(k) number K901550. 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 IVAC(R) SYRINGE PUMP - MODEL 770?

IVAC(R) SYRINGE PUMP - MODEL 770 is a medical device that received FDA 510(k) clearance on 1990-10-04. The listed applicant is Y. The 510(k) number is K901550.

When did IVAC(R) SYRINGE PUMP - MODEL 770 receive FDA 510(k) clearance?

IVAC(R) SYRINGE PUMP - MODEL 770 received FDA 510(k) clearance on 1990-10-04, under 510(k) number K901550.

Who is the listed applicant for IVAC(R) SYRINGE PUMP - MODEL 770?

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

What is the FDA product code for IVAC(R) SYRINGE PUMP - MODEL 770?

The FDA product code for IVAC(R) SYRINGE PUMP - MODEL 770 is FRN.

Related Clinical Trials

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.

Other records listing Y 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.

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Related Devices (Code: FRN)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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