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FDA 510(k)

FLEXIFLO ENTERAL PUMP SET

K-Number: K791531 · 1979-09-12

ApplicantAbbott Laboratories
Decision Date1979-09-12
Product CodeBSS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FLEXIFLO ENTERAL PUMP SET is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1979-09-12 under 510(k) number K791531. The device is classified under product code BSS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIFLO ENTERAL PUMP SET?

FLEXIFLO ENTERAL PUMP SET is a medical device that received FDA 510(k) clearance on 1979-09-12. The listed applicant is Abbott Laboratories. The 510(k) number is K791531.

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

FLEXIFLO ENTERAL PUMP SET received FDA 510(k) clearance on 1979-09-12, under 510(k) number K791531.

Who is the listed applicant for FLEXIFLO ENTERAL PUMP SET?

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

What is the FDA product code for FLEXIFLO ENTERAL PUMP SET?

The FDA product code for FLEXIFLO ENTERAL PUMP SET is BSS.

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Related Devices (Code: BSS)

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.

K051480ENTERAL FEEDING TUBEBiosearch Medical Products, Inc.K984629MOSS TUBES, INC. NASAL TUBE - MARK IVMoss Tubes, Inc.K961711ASPISAFE GASTRIC TUBEB.Braun Medical, Inc.K933596GASTRIC, CATHETER, IRRIGATION & ASPIRATIONPolamedco, Inc.K930510RADIUS ENTERAL FEEDING TUBERadius Intl., Inc.K935688AN-10S ANDERSEN TUBE WITH STYLETH.W. Andersen Products, 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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