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FDA 510(k)

SYRINGE INFUSION PUMP #2716

K-Number: K801904 · 1980-08-27

ApplicantHarvard Apparatus, Inc.
Decision Date1980-08-27
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SYRINGE INFUSION PUMP #2716 is the device name listed in this FDA 510(k) record. The listed applicant is Harvard Apparatus, Inc.. It received FDA 510(k) clearance on 1980-08-27 under 510(k) number K801904. 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 SYRINGE INFUSION PUMP #2716?

SYRINGE INFUSION PUMP #2716 is a medical device that received FDA 510(k) clearance on 1980-08-27. The listed applicant is Harvard Apparatus, Inc.. The 510(k) number is K801904.

When did SYRINGE INFUSION PUMP #2716 receive FDA 510(k) clearance?

SYRINGE INFUSION PUMP #2716 received FDA 510(k) clearance on 1980-08-27, under 510(k) number K801904.

Who is the listed applicant for SYRINGE INFUSION PUMP #2716?

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

What is the FDA product code for SYRINGE INFUSION PUMP #2716?

The FDA product code for SYRINGE INFUSION PUMP #2716 is FRN.

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Other records listing Harvard Apparatus, 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.

K970678THE HARVARD LIBRARYK952794HARVARD 2 SYRINGE PUMPK903614HARVARD/LTE LABORATORY STEAM STERILIZER AUTOCLAVEK903613HARVARD/LTE BENCHTOP STEAM STERILIZER (AUTOCLAVE)K813644MODEL 2650 HIGH CAPACITY DUAL SYRINGEK800569SYRINGE INFUSION PUMP #2720

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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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