FDA 510(k)

BONN MICRO IRIS HOOK (NON-STERILE) #7613

K-Number: K801469 · 1980-07-28

Decision Date1980-07-28

Product CodeHNQ

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

BONN MICRO IRIS HOOK (NON-STERILE) #7613 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 1980-07-28 under 510(k) number K801469. The device is classified under product code HNQ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BONN MICRO IRIS HOOK (NON-STERILE) #7613?

BONN MICRO IRIS HOOK (NON-STERILE) #7613 is a medical device that received FDA 510(k) clearance on 1980-07-28. The listed applicant is Edward Weck, Inc.. The 510(k) number is K801469.

When did BONN MICRO IRIS HOOK (NON-STERILE) #7613 receive FDA 510(k) clearance?

BONN MICRO IRIS HOOK (NON-STERILE) #7613 received FDA 510(k) clearance on 1980-07-28, under 510(k) number K801469.

Who is the listed applicant for BONN MICRO IRIS HOOK (NON-STERILE) #7613?

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 BONN MICRO IRIS HOOK (NON-STERILE) #7613?

The FDA product code for BONN MICRO IRIS HOOK (NON-STERILE) #7613 is HNQ.

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Related Devices (Code: HNQ)

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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.