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FDA 510(k)

MODEL 27080 CALCUTRIPT ELECTROHYDRAULIC LITHR SYS

K-Number: K883189 · 1989-02-13

ApplicantKARL STORZ Endoscopy-America, Inc.
Decision Date1989-02-13
Product CodeFFK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODEL 27080 CALCUTRIPT ELECTROHYDRAULIC LITHR SYS is the device name listed in this FDA 510(k) record. The listed applicant is KARL STORZ Endoscopy-America, Inc.. It received FDA 510(k) clearance on 1989-02-13 under 510(k) number K883189. The device is classified under product code FFK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 27080 CALCUTRIPT ELECTROHYDRAULIC LITHR SYS?

MODEL 27080 CALCUTRIPT ELECTROHYDRAULIC LITHR SYS is a medical device that received FDA 510(k) clearance on 1989-02-13. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K883189.

When did MODEL 27080 CALCUTRIPT ELECTROHYDRAULIC LITHR SYS receive FDA 510(k) clearance?

MODEL 27080 CALCUTRIPT ELECTROHYDRAULIC LITHR SYS received FDA 510(k) clearance on 1989-02-13, under 510(k) number K883189.

Who is the listed applicant for MODEL 27080 CALCUTRIPT ELECTROHYDRAULIC LITHR SYS?

The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 27080 CALCUTRIPT ELECTROHYDRAULIC LITHR SYS?

The FDA product code for MODEL 27080 CALCUTRIPT ELECTROHYDRAULIC LITHR SYS is FFK.

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Other records listing KARL STORZ Endoscopy-America, Inc. 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.

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Related Devices (Code: FFK)

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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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