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FDA 510(k)

HUNTLEIGH FLOWTRON AIR HAND GARMENT, HG300

K-Number: K850945 · 1985-08-20

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

Device Summary

HUNTLEIGH FLOWTRON AIR HAND GARMENT, HG300 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 K850945. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUNTLEIGH FLOWTRON AIR HAND GARMENT, HG300?

HUNTLEIGH FLOWTRON AIR HAND GARMENT, HG300 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 K850945.

When did HUNTLEIGH FLOWTRON AIR HAND GARMENT, HG300 receive FDA 510(k) clearance?

HUNTLEIGH FLOWTRON AIR HAND GARMENT, HG300 received FDA 510(k) clearance on 1985-08-20, under 510(k) number K850945.

Who is the listed applicant for HUNTLEIGH FLOWTRON AIR HAND GARMENT, HG300?

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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