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FDA 510(k)

DRI-CLAVE LIQUID KLEENZALL

K-Number: K880754 · 1988-05-12

ApplicantColumbus Dental Mfg. Co.
Decision Date1988-05-12
Product CodeEHZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DRI-CLAVE LIQUID KLEENZALL is the device name listed in this FDA 510(k) record. The listed applicant is Columbus Dental Mfg. Co.. It received FDA 510(k) clearance on 1988-05-12 under 510(k) number K880754. The device is classified under product code EHZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRI-CLAVE LIQUID KLEENZALL?

DRI-CLAVE LIQUID KLEENZALL is a medical device that received FDA 510(k) clearance on 1988-05-12. The listed applicant is Columbus Dental Mfg. Co.. The 510(k) number is K880754.

When did DRI-CLAVE LIQUID KLEENZALL receive FDA 510(k) clearance?

DRI-CLAVE LIQUID KLEENZALL received FDA 510(k) clearance on 1988-05-12, under 510(k) number K880754.

Who is the listed applicant for DRI-CLAVE LIQUID KLEENZALL?

The FDA 510(k) record lists Columbus Dental Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRI-CLAVE LIQUID KLEENZALL?

The FDA product code for DRI-CLAVE LIQUID KLEENZALL is EHZ.

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Other records listing Columbus Dental Mfg. Co. 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.

K880607UTILITY WAX STRIPS, SPEARMINTK880606UTILITY WAX STRIPS, CINNAMONK872243PEKALUX(TM)K871164GLUMA(TM) BONDING SYSTEMK872272PEKALUX/GLUMA LIGHT CURED ANTERIOR RESTORATIVE SYSK871165LUMIFOR(TM) COMPOSITE

View all 11 devices →

Related Devices (Code: EHZ)

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.

K973248IMTEC BONE COLLECTOR SYSTEMImtec Corp.K941164TAP EXPRESS EJECTORTap Express, Inc.K911072SUPER EVACRETRACTOR, DISPOSABLE ORAL EVACUATORA & F ProductsK903718OROSCOPE MODEL NUMBER COS-100Cygnus Instruments, Inc.K892881DENTAL SANI-SLEEVE STERILE 60MM X 1650MM #1101Nieusma R & D, Inc.K892882DENTAL SANI-SLEEVE STERILE 100MM X 2200MM #1102Nieusma R & D, Inc.

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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