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FDA 510(k)

VALLEYLAB MODEL IV7200 INFUSION PUMP

K-Number: K873161 · 1987-11-05

ApplicantValleylab, Inc.
Decision Date1987-11-05
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VALLEYLAB MODEL IV7200 INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1987-11-05 under 510(k) number K873161. 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 VALLEYLAB MODEL IV7200 INFUSION PUMP?

VALLEYLAB MODEL IV7200 INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1987-11-05. The listed applicant is Valleylab, Inc.. The 510(k) number is K873161.

When did VALLEYLAB MODEL IV7200 INFUSION PUMP receive FDA 510(k) clearance?

VALLEYLAB MODEL IV7200 INFUSION PUMP received FDA 510(k) clearance on 1987-11-05, under 510(k) number K873161.

Who is the listed applicant for VALLEYLAB MODEL IV7200 INFUSION PUMP?

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

What is the FDA product code for VALLEYLAB MODEL IV7200 INFUSION PUMP?

The FDA product code for VALLEYLAB MODEL IV7200 INFUSION PUMP is FRN.

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Other records listing Valleylab, 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.

K031011LIGASURE 5MM LAPAROSCOPIC SEALER-DIVIDER, MODEL LS1500K010010VALLEYLAB LIGASURE PRECISE INSTRUMENT VESSEL SEALING SYSTEM-MODEL # LS1200 & SLIGAURE GENERATORK010013LIGASURE LAPAROSCOPIC SEALER DIVIDER MODEL LS1100K994428E7512 PREMIE REM POLYHESIVE II PATIENT RETURN ELECTRODEK983743BISURE LAPAROSCOPIC BIPOLAR FORCEPSK981916LIGASURE VESSEL SEALING SYSTEM

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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.

K253703RemunityPRO+ Pump for Remodulin® (treprostinil) InjectionDeka R&D CorpK252015FreedomEdge Infusion System; High-Flo SubQ Needle Set; Precision Flow Rate TubingKoru Medical Systems, Inc.K251636Spectrum IQ Infusion System with Dose IQ Safety Software (3570009)Baxter Healthcare CorporationK251640SIGMA Spectrum Infusion Pump with Master Drug LibraryBaxter Healthcare CorporationK242752MRidium 3870 MRI Infusion Pump System (3870)Iradimed CorporationK243855BD Alaris Infusion System with Guardrails Suite MXCarefusion 303, Inc.

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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