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FDA 510(k)

STORZ S2060-C & DP9040 BIPOLAR CCORD ADAPTORS

K-Number: K954253 · 1995-11-01

ApplicantStorz Instrument Co.
Decision Date1995-11-01
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STORZ S2060-C & DP9040 BIPOLAR CCORD ADAPTORS is the device name listed in this FDA 510(k) record. The listed applicant is Storz Instrument Co.. It received FDA 510(k) clearance on 1995-11-01 under 510(k) number K954253. 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 STORZ S2060-C & DP9040 BIPOLAR CCORD ADAPTORS?

STORZ S2060-C & DP9040 BIPOLAR CCORD ADAPTORS is a medical device that received FDA 510(k) clearance on 1995-11-01. The listed applicant is Storz Instrument Co.. The 510(k) number is K954253.

When did STORZ S2060-C & DP9040 BIPOLAR CCORD ADAPTORS receive FDA 510(k) clearance?

STORZ S2060-C & DP9040 BIPOLAR CCORD ADAPTORS received FDA 510(k) clearance on 1995-11-01, under 510(k) number K954253.

Who is the listed applicant for STORZ S2060-C & DP9040 BIPOLAR CCORD ADAPTORS?

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

What is the FDA product code for STORZ S2060-C & DP9040 BIPOLAR CCORD ADAPTORS?

The FDA product code for STORZ S2060-C & DP9040 BIPOLAR CCORD ADAPTORS is GEI.

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Other records listing Storz Instrument Co. as applicant

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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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