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FDA 510(k)

RAPIDEX BIOLOGICAL SURFACTANT

K-Number: K862282 · 1987-05-11

ApplicantRapidex of London
Decision Date1987-05-11
Product CodeFLG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RAPIDEX BIOLOGICAL SURFACTANT is the device name listed in this FDA 510(k) record. The listed applicant is Rapidex of London. It received FDA 510(k) clearance on 1987-05-11 under 510(k) number K862282. The device is classified under product code FLG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAPIDEX BIOLOGICAL SURFACTANT?

RAPIDEX BIOLOGICAL SURFACTANT is a medical device that received FDA 510(k) clearance on 1987-05-11. The listed applicant is Rapidex of London. The 510(k) number is K862282.

When did RAPIDEX BIOLOGICAL SURFACTANT receive FDA 510(k) clearance?

RAPIDEX BIOLOGICAL SURFACTANT received FDA 510(k) clearance on 1987-05-11, under 510(k) number K862282.

Who is the listed applicant for RAPIDEX BIOLOGICAL SURFACTANT?

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

What is the FDA product code for RAPIDEX BIOLOGICAL SURFACTANT?

The FDA product code for RAPIDEX BIOLOGICAL SURFACTANT is FLG.

Related Clinical Trials

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Related Devices (Code: FLG)

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.

K944950KLENZYMECalgon Corp.K944494ALSA-KLENZCalgon Vestal Div.K944033BILL EVANS-KLENZCalgon Vestal Div.K940263NPH-KLENZCalgon Corp.K941163MON-KLENZCalgon Vestal Div.K935063INSTRU KLENZCalgon Corp.

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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