FDA 510(k)

DTF-1000LL,DTF-1000

K-Number: K911118 · 1991-11-20

Decision Date1991-11-20

Product CodeEIB

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

DTF-1000LL,DTF-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Cp Medical. It received FDA 510(k) clearance on 1991-11-20 under 510(k) number K911118. The device is classified under product code EIB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DTF-1000LL,DTF-1000?

DTF-1000LL,DTF-1000 is a medical device that received FDA 510(k) clearance on 1991-11-20. The listed applicant is Cp Medical. The 510(k) number is K911118.

When did DTF-1000LL,DTF-1000 receive FDA 510(k) clearance?

DTF-1000LL,DTF-1000 received FDA 510(k) clearance on 1991-11-20, under 510(k) number K911118.

Who is the listed applicant for DTF-1000LL,DTF-1000?

The FDA 510(k) record lists Cp Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DTF-1000LL,DTF-1000?

The FDA product code for DTF-1000LL,DTF-1000 is EIB.

Other records listing Cp Medical 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.

K094028CP-FIBER (ORTHOFIBER)K072229MONOSWIFT K071550PRE-WAXED NEEDLES WITH GOLD FIDUCIARY MARKERS K060987OSCERA7 SYNTHETIC ABSORBABLE BONE WAX, MODEL OS31 K041894ORTHOFIBER K034062CP SLEEVE AND RIVER SLEEVE

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Related Devices (Code: EIB)

K874543MODEL OPO-32 IRRIGATION SLEEVEAllergan, Inc.K822411SYSTEM 80 FACEPLATE-IN-THE-EAR #F1Western Advanced Technology, Inc.K760570ROBINSON MIDDLE EAR PROSTHESISXomed, 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.