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FDA 510(k)

FRAZIER-FERGUSON SUCTION TUBES

K-Number: K801468 · 1980-08-12

ApplicantEdward Weck, Inc.
Decision Date1980-08-12
Product CodeKCB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FRAZIER-FERGUSON SUCTION TUBES 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 1980-08-12 under 510(k) number K801468. The device is classified under product code KCB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRAZIER-FERGUSON SUCTION TUBES?

FRAZIER-FERGUSON SUCTION TUBES is a medical device that received FDA 510(k) clearance on 1980-08-12. The listed applicant is Edward Weck, Inc.. The 510(k) number is K801468.

When did FRAZIER-FERGUSON SUCTION TUBES receive FDA 510(k) clearance?

FRAZIER-FERGUSON SUCTION TUBES received FDA 510(k) clearance on 1980-08-12, under 510(k) number K801468.

Who is the listed applicant for FRAZIER-FERGUSON SUCTION TUBES?

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 FRAZIER-FERGUSON SUCTION TUBES?

The FDA product code for FRAZIER-FERGUSON SUCTION TUBES is KCB.

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Other records listing Edward Weck, 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.

K915378WECK TROCARK914690LM15(TM), CATALOG NUMBER - 523821K911915HEMOCLIP IIK914470PNEUMO-SEAL(TM)K911272ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705K902108HEM-O-LOK(TM)

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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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