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FDA 510(k)

INFUSION PUMP RETROGRADE EXTEN. AS 715

K-Number: K830654 · 1983-03-24

Decision Date1983-03-24
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFUSION PUMP RETROGRADE EXTEN. AS 715 is the device name listed in this FDA 510(k) record. The listed applicant is Narco Scientific. It received FDA 510(k) clearance on 1983-03-24 under 510(k) number K830654. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFUSION PUMP RETROGRADE EXTEN. AS 715?

INFUSION PUMP RETROGRADE EXTEN. AS 715 is a medical device that received FDA 510(k) clearance on 1983-03-24. The listed applicant is Narco Scientific. The 510(k) number is K830654.

When did INFUSION PUMP RETROGRADE EXTEN. AS 715 receive FDA 510(k) clearance?

INFUSION PUMP RETROGRADE EXTEN. AS 715 received FDA 510(k) clearance on 1983-03-24, under 510(k) number K830654.

Who is the listed applicant for INFUSION PUMP RETROGRADE EXTEN. AS 715?

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

What is the FDA product code for INFUSION PUMP RETROGRADE EXTEN. AS 715?

The FDA product code for INFUSION PUMP RETROGRADE EXTEN. AS 715 is FPA.

Related Clinical Trials

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.

Other records listing Narco Scientific 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.

View all 30 devices →

Related Devices (Code: FPA)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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