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FDA 510(k)

HUNTLEIGH BETA II HM85

K-Number: K870681 · 1987-03-04

ApplicantHuntleigh Technology, Inc.
Decision Date1987-03-04
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HUNTLEIGH BETA II HM85 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 1987-03-04 under 510(k) number K870681. The device is classified under product code FNM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUNTLEIGH BETA II HM85?

HUNTLEIGH BETA II HM85 is a medical device that received FDA 510(k) clearance on 1987-03-04. The listed applicant is Huntleigh Technology, Inc.. The 510(k) number is K870681.

When did HUNTLEIGH BETA II HM85 receive FDA 510(k) clearance?

HUNTLEIGH BETA II HM85 received FDA 510(k) clearance on 1987-03-04, under 510(k) number K870681.

Who is the listed applicant for HUNTLEIGH BETA II HM85?

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

What is the FDA product code for HUNTLEIGH BETA II HM85?

The FDA product code for HUNTLEIGH BETA II HM85 is FNM.

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Other records listing Huntleigh Technology, Inc. as applicant

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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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