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FDA 510(k)

ENTERAL NUTRITION PUMP

K-Number: K841630 · 1984-06-07

ApplicantSuperior Plastic Products Corp.
Decision Date1984-06-07
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ENTERAL NUTRITION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Superior Plastic Products Corp.. It received FDA 510(k) clearance on 1984-06-07 under 510(k) number K841630. 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 ENTERAL NUTRITION PUMP?

ENTERAL NUTRITION PUMP is a medical device that received FDA 510(k) clearance on 1984-06-07. The listed applicant is Superior Plastic Products Corp.. The 510(k) number is K841630.

When did ENTERAL NUTRITION PUMP receive FDA 510(k) clearance?

ENTERAL NUTRITION PUMP received FDA 510(k) clearance on 1984-06-07, under 510(k) number K841630.

Who is the listed applicant for ENTERAL NUTRITION PUMP?

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

What is the FDA product code for ENTERAL NUTRITION PUMP?

The FDA product code for ENTERAL NUTRITION PUMP is FRN.

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Other records listing Superior Plastic Products Corp. 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.

K851981NO. 5300-3 1/2 FRENCH UMBILICAL VESSEL CATH. ETC.K8439759 FRENCH 42LONG POLYURETHANE GRADUATED ENTERIC FEK841945ENTERAL FEEDING BOTTLEK841480INFECTION CONTROL VALVEK840323SILICONE SUCTION & IRRIGATION DRAINK840324SILICONE SUMP DRAIN 20 & 40 FRENCH

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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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