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FDA 510(k)

ENDOSCOPE

K-Number: K935818 · 1994-07-13

ApplicantCuda Products Co.
Decision Date1994-07-13
Product CodeGDB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Cuda Products Co.. It received FDA 510(k) clearance on 1994-07-13 under 510(k) number K935818. The device is classified under product code GDB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPE?

ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1994-07-13. The listed applicant is Cuda Products Co.. The 510(k) number is K935818.

When did ENDOSCOPE receive FDA 510(k) clearance?

ENDOSCOPE received FDA 510(k) clearance on 1994-07-13, under 510(k) number K935818.

Who is the listed applicant for ENDOSCOPE?

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

What is the FDA product code for ENDOSCOPE?

The FDA product code for ENDOSCOPE is GDB.

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Other records listing Cuda Products Co. 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.

K983277LIGHTSOURCE OR ILLUMINATOR MODEL I-100K981962CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCEK981469CERMAX300 LIGHTSOURCEK980350VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150K980166LIGHTSOURCE OR ILLUMINATORK961074LIGHTSOURCE OR ILLUMINATOR

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Related Devices (Code: GDB)

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.

K032283DESIGNS FOR VISION FIBEROPTIC LIGHTDesigns For Vision, Inc.K961536FLEXSCOPEMatrix Medica, Inc.K882061OLYMPUS GF-UM3/EU-M3Olympus Corp.K855151FRITCH OPHTHALMIC ENDOSCOPERegtecK843900FOCUSCOPE UNIVERSAL SYSTEMMedical Diagnostics, Ca.K810007PENTAX UPPER G.I. FIBERSCOPE, #FG-34Pentax Precision Instrument Corp.

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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