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FDA 510(k)

OLYMPUS CHP-P10 NEPHROSCOPE/CYSTOSCOPE

K-Number: K843084 · 1985-01-03

ApplicantOlympus Corp.
Decision Date1985-01-03
Product CodeFBO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OLYMPUS CHP-P10 NEPHROSCOPE/CYSTOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1985-01-03 under 510(k) number K843084. The device is classified under product code FBO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS CHP-P10 NEPHROSCOPE/CYSTOSCOPE?

OLYMPUS CHP-P10 NEPHROSCOPE/CYSTOSCOPE is a medical device that received FDA 510(k) clearance on 1985-01-03. The listed applicant is Olympus Corp.. The 510(k) number is K843084.

When did OLYMPUS CHP-P10 NEPHROSCOPE/CYSTOSCOPE receive FDA 510(k) clearance?

OLYMPUS CHP-P10 NEPHROSCOPE/CYSTOSCOPE received FDA 510(k) clearance on 1985-01-03, under 510(k) number K843084.

Who is the listed applicant for OLYMPUS CHP-P10 NEPHROSCOPE/CYSTOSCOPE?

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

What is the FDA product code for OLYMPUS CHP-P10 NEPHROSCOPE/CYSTOSCOPE?

The FDA product code for OLYMPUS CHP-P10 NEPHROSCOPE/CYSTOSCOPE is FBO.

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Other records listing Olympus Corp. 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.

K915402EW-10 AND EW-20K933200OLYMPUS PBD STENTSK942338OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIESK931763HF-RESECTION ELECTRODE, LOOP W/RUNNER ENDOS/ACCESSK934835FLOVALK931764HF RESECTION ELECTRODE, LOOP W/RUNNER HYSTER/ACCES

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Related Devices (Code: FBO)

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.

K244001KARL STORZ Cysto-Urethro-Fiberscope (11272CU1); KARL STORZ Cysto-Urethro-Fiberscope (11272C2)Karl Storz SE & CO. KGK243409KARL STORZ Pediatric Cysto-Urethro-Fiberscope (11274BCU1)Karl Storz SE & CO. KGK082046KARL STORZ PEDIATRIC FLEXIBLE CYSTO-URETHRO-FIBERSCOPE, MODEL 11278C1/ACUI AND CIRCON AUR-735 PEDIATRIC CYSTOURETHEROSCOKARL STORZ Endoscopy-America, Inc.K080780ANCHORAGE SCOPE, MODEL 000003Epitek, Inc.K062918KARL STORZ FLEXIBLE VIDEO-URETHRO-CYSTOSCOPE SYSTEMKARL STORZ Endoscopy-America, Inc.K061646LASERSCOPE GUIDED DELIVERY DEVICE (GDD) CYSTOURETHROSCOPE & ACCESSORIESLaserscope

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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