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FDA 510(k)

DUOWIPE CAUTERY TIP & INSTRUMENT CLEANER

K-Number: K830277 · 1983-03-08

ApplicantRitmed, Inc.
Decision Date1983-03-08
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DUOWIPE CAUTERY TIP & INSTRUMENT CLEANER is the device name listed in this FDA 510(k) record. The listed applicant is Ritmed, Inc.. It received FDA 510(k) clearance on 1983-03-08 under 510(k) number K830277. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUOWIPE CAUTERY TIP & INSTRUMENT CLEANER?

DUOWIPE CAUTERY TIP & INSTRUMENT CLEANER is a medical device that received FDA 510(k) clearance on 1983-03-08. The listed applicant is Ritmed, Inc.. The 510(k) number is K830277.

When did DUOWIPE CAUTERY TIP & INSTRUMENT CLEANER receive FDA 510(k) clearance?

DUOWIPE CAUTERY TIP & INSTRUMENT CLEANER received FDA 510(k) clearance on 1983-03-08, under 510(k) number K830277.

Who is the listed applicant for DUOWIPE CAUTERY TIP & INSTRUMENT CLEANER?

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

What is the FDA product code for DUOWIPE CAUTERY TIP & INSTRUMENT CLEANER?

The FDA product code for DUOWIPE CAUTERY TIP & INSTRUMENT CLEANER is GEI.

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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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