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FDA 510(k)

MODEL 2231 CO2 INSUFFLATOR

K-Number: K934884 · 1995-02-07

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1995-02-07
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MODEL 2231 CO2 INSUFFLATOR is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1995-02-07 under 510(k) number K934884. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 2231 CO2 INSUFFLATOR?

MODEL 2231 CO2 INSUFFLATOR is a medical device that received FDA 510(k) clearance on 1995-02-07. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K934884.

When did MODEL 2231 CO2 INSUFFLATOR receive FDA 510(k) clearance?

MODEL 2231 CO2 INSUFFLATOR received FDA 510(k) clearance on 1995-02-07, under 510(k) number K934884.

Who is the listed applicant for MODEL 2231 CO2 INSUFFLATOR?

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

What is the FDA product code for MODEL 2231 CO2 INSUFFLATOR?

The FDA product code for MODEL 2231 CO2 INSUFFLATOR is HIF.

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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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