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FDA 510(k)

STERILIZING CASE CAT. NO. 65199

K-Number: K800080 · 1980-01-28

ApplicantEdward Weck, Inc.
Decision Date1980-01-28
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILIZING CASE CAT. NO. 65199 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 1980-01-28 under 510(k) number K800080. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILIZING CASE CAT. NO. 65199?

STERILIZING CASE CAT. NO. 65199 is a medical device that received FDA 510(k) clearance on 1980-01-28. The listed applicant is Edward Weck, Inc.. The 510(k) number is K800080.

When did STERILIZING CASE CAT. NO. 65199 receive FDA 510(k) clearance?

STERILIZING CASE CAT. NO. 65199 received FDA 510(k) clearance on 1980-01-28, under 510(k) number K800080.

Who is the listed applicant for STERILIZING CASE CAT. NO. 65199?

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 STERILIZING CASE CAT. NO. 65199?

The FDA product code for STERILIZING CASE CAT. NO. 65199 is FLE.

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Other records listing Edward Weck, Inc. as applicant

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Related Devices (Code: FLE)

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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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