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FDA 510(k)

QWIKSPIN (TM)

K-Number: K860172 · 1986-02-11

ApplicantNorfolk Scientific, Inc.
Decision Date1986-02-11
Product CodeJQC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QWIKSPIN (TM) is the device name listed in this FDA 510(k) record. The listed applicant is Norfolk Scientific, Inc.. It received FDA 510(k) clearance on 1986-02-11 under 510(k) number K860172. The device is classified under product code JQC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QWIKSPIN (TM)?

QWIKSPIN (TM) is a medical device that received FDA 510(k) clearance on 1986-02-11. The listed applicant is Norfolk Scientific, Inc.. The 510(k) number is K860172.

When did QWIKSPIN (TM) receive FDA 510(k) clearance?

QWIKSPIN (TM) received FDA 510(k) clearance on 1986-02-11, under 510(k) number K860172.

Who is the listed applicant for QWIKSPIN (TM)?

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

What is the FDA product code for QWIKSPIN (TM)?

The FDA product code for QWIKSPIN (TM) is JQC.

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Other records listing Norfolk Scientific, 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.

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Related Devices (Code: JQC)

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

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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