FDA 510(k)

CMI E-Z FLO BULB P.N. 701

K-Number: K932128 · 1994-04-07

ApplicantColumbia Medical & Surgical, Inc.

Decision Date1994-04-07

Product CodeFFY

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

CMI E-Z FLO BULB P.N. 701 is the device name listed in this FDA 510(k) record. The listed applicant is Columbia Medical & Surgical, Inc.. It received FDA 510(k) clearance on 1994-04-07 under 510(k) number K932128. The device is classified under product code FFY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CMI E-Z FLO BULB P.N. 701?

CMI E-Z FLO BULB P.N. 701 is a medical device that received FDA 510(k) clearance on 1994-04-07. The listed applicant is Columbia Medical & Surgical, Inc.. The 510(k) number is K932128.

When did CMI E-Z FLO BULB P.N. 701 receive FDA 510(k) clearance?

CMI E-Z FLO BULB P.N. 701 received FDA 510(k) clearance on 1994-04-07, under 510(k) number K932128.

Who is the listed applicant for CMI E-Z FLO BULB P.N. 701?

The FDA 510(k) record lists Columbia Medical & Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CMI E-Z FLO BULB P.N. 701?

The FDA product code for CMI E-Z FLO BULB P.N. 701 is FFY.

Other records listing Columbia Medical & Surgical, 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.

K942725CMI VELVET TOUCH VACUUM EXTRACTOR K914552CMI VACUUM PUMP K915763MODIFIED DISPOSABLE FETAL VACUUM

Related Devices (Code: FFY)

K900781WORKING CHANNEL VALVEApplied Urology, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.