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FDA 510(k)

BOWIE-DICK TEST CARD CATALOG NUMBER 008018

K-Number: K897045 · 1990-02-15

ApplicantEdward Weck, Inc.
Decision Date1990-02-15
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BOWIE-DICK TEST CARD CATALOG NUMBER 008018 is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1990-02-15 under 510(k) number K897045. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOWIE-DICK TEST CARD CATALOG NUMBER 008018?

BOWIE-DICK TEST CARD CATALOG NUMBER 008018 is a medical device that received FDA 510(k) clearance on 1990-02-15. The listed applicant is Edward Weck, Inc.. The 510(k) number is K897045.

When did BOWIE-DICK TEST CARD CATALOG NUMBER 008018 receive FDA 510(k) clearance?

BOWIE-DICK TEST CARD CATALOG NUMBER 008018 received FDA 510(k) clearance on 1990-02-15, under 510(k) number K897045.

Who is the listed applicant for BOWIE-DICK TEST CARD CATALOG NUMBER 008018?

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

What is the FDA product code for BOWIE-DICK TEST CARD CATALOG NUMBER 008018?

The FDA product code for BOWIE-DICK TEST CARD CATALOG NUMBER 008018 is JOJ.

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Related Devices (Code: JOJ)

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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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