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FDA 510(k)

REAL FIBER OPTIC URETERAL TRANSILLUMIN

K-Number: K834576 · 1984-04-20

ApplicantDouglas Manufacturer Co.
Decision Date1984-04-20
Product CodeFFS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

REAL FIBER OPTIC URETERAL TRANSILLUMIN is the device name listed in this FDA 510(k) record. The listed applicant is Douglas Manufacturer Co.. It received FDA 510(k) clearance on 1984-04-20 under 510(k) number K834576. The device is classified under product code FFS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REAL FIBER OPTIC URETERAL TRANSILLUMIN?

REAL FIBER OPTIC URETERAL TRANSILLUMIN is a medical device that received FDA 510(k) clearance on 1984-04-20. The listed applicant is Douglas Manufacturer Co.. The 510(k) number is K834576.

When did REAL FIBER OPTIC URETERAL TRANSILLUMIN receive FDA 510(k) clearance?

REAL FIBER OPTIC URETERAL TRANSILLUMIN received FDA 510(k) clearance on 1984-04-20, under 510(k) number K834576.

Who is the listed applicant for REAL FIBER OPTIC URETERAL TRANSILLUMIN?

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

What is the FDA product code for REAL FIBER OPTIC URETERAL TRANSILLUMIN?

The FDA product code for REAL FIBER OPTIC URETERAL TRANSILLUMIN is FFS.

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Related Devices (Code: FFS)

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.

K072521COOK FIBER OPTIC BUNDLE AND FLEXOR DEFLECTING ACCESS SHEATHCook Urological, Inc.K061622PS SERIESPhotonic Optische Gerate Gesmbh & CokgK063309TRU-CABLETruphatek International, Ltd.K061025ACCUTECH ENDOLITE PROBEAccutech Medical Technologies, Inc.K023633SOVIS OPTIQUE'S ENDOSCOPIC CABLESovis OptiqueK001698MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159Cogent Light Technologies, Inc.

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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