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FDA 510(k)

QWIK-CALL

K-Number: K860052 · 1986-02-06

ApplicantEmde Corp.
Decision Date1986-02-06
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

QWIK-CALL is the device name listed in this FDA 510(k) record. The listed applicant is Emde Corp.. It received FDA 510(k) clearance on 1986-02-06 under 510(k) number K860052. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QWIK-CALL?

QWIK-CALL is a medical device that received FDA 510(k) clearance on 1986-02-06. The listed applicant is Emde Corp.. The 510(k) number is K860052.

When did QWIK-CALL receive FDA 510(k) clearance?

QWIK-CALL received FDA 510(k) clearance on 1986-02-06, under 510(k) number K860052.

Who is the listed applicant for QWIK-CALL?

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

What is the FDA product code for QWIK-CALL?

The FDA product code for QWIK-CALL is KNT.

Other records listing Emde Corp. 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.

K811199MARZ-175K791465MOSQUITO ARTERIAL BLOOD SAMPLERK771013MOSQUITO

Related Devices (Code: KNT)

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.

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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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