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FDA 510(k)

IVAC SYRING PUMP MODEL 770

K-Number: K925091 · 1993-07-08

ApplicantY
Decision Date1993-07-08
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IVAC SYRING 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 1993-07-08 under 510(k) number K925091. 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 SYRING PUMP MODEL 770?

IVAC SYRING PUMP MODEL 770 is a medical device that received FDA 510(k) clearance on 1993-07-08. The listed applicant is Y. The 510(k) number is K925091.

When did IVAC SYRING PUMP MODEL 770 receive FDA 510(k) clearance?

IVAC SYRING PUMP MODEL 770 received FDA 510(k) clearance on 1993-07-08, under 510(k) number K925091.

Who is the listed applicant for IVAC SYRING 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 SYRING PUMP MODEL 770?

The FDA product code for IVAC SYRING PUMP MODEL 770 is FRN.

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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.

K955846MODEL 2082 TEMP PLUS III THERMOMETER/MODEL 2087 TEMP PLUS III WALL MOUNT THERMOMETERK960280IVAC NEEDLE FREE VALVE ADMINISTRATION SETSK953225IVAC BALL VALCE ADMIN. SETSK934095IVAC VENTED SYRINGE ADAPTER ADMINISTRATION SETSK940897IVAC NEEDLELESS INFECTION VALVE ADMINISTRATION SETK931550EZ ADMINISTRATION SET

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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.

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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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