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FDA 510(k)

HUNTLEIGH FLOWTRON AIR, AC400/2 AIR

K-Number: K850910 · 1985-08-20

ApplicantHuntleigh Technology, Inc.
Decision Date1985-08-20
Product Code
DecisionSubstantially Equivalent

Device Summary

HUNTLEIGH FLOWTRON AIR, AC400/2 AIR is the device name listed in this FDA 510(k) record. The listed applicant is Huntleigh Technology, Inc.. It received FDA 510(k) clearance on 1985-08-20 under 510(k) number K850910. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUNTLEIGH FLOWTRON AIR, AC400/2 AIR?

HUNTLEIGH FLOWTRON AIR, AC400/2 AIR is a medical device that received FDA 510(k) clearance on 1985-08-20. The listed applicant is Huntleigh Technology, Inc.. The 510(k) number is K850910.

When did HUNTLEIGH FLOWTRON AIR, AC400/2 AIR receive FDA 510(k) clearance?

HUNTLEIGH FLOWTRON AIR, AC400/2 AIR received FDA 510(k) clearance on 1985-08-20, under 510(k) number K850910.

Who is the listed applicant for HUNTLEIGH FLOWTRON AIR, AC400/2 AIR?

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

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Other records listing Huntleigh Technology, 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.

K992733AKRON ATP9 TRACTION MACHINEK964699RHEO DOPPLEX II (RD 2)K924516OP3/VP4K910188FLOWPLUS AC330 PUMP GARMENTSK900882MULTI DOPPLEX, MD-1K900618HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140

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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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