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FDA 510(k)

VIDEO ENDOSCOPE-RIGID MODIFICATION

K-Number: K921294 · 1994-07-20

ApplicantMedical Dynamics, Inc.
Decision Date1994-07-20
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

VIDEO ENDOSCOPE-RIGID MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Medical Dynamics, Inc.. It received FDA 510(k) clearance on 1994-07-20 under 510(k) number K921294. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIDEO ENDOSCOPE-RIGID MODIFICATION?

VIDEO ENDOSCOPE-RIGID MODIFICATION is a medical device that received FDA 510(k) clearance on 1994-07-20. The listed applicant is Medical Dynamics, Inc.. The 510(k) number is K921294.

When did VIDEO ENDOSCOPE-RIGID MODIFICATION receive FDA 510(k) clearance?

VIDEO ENDOSCOPE-RIGID MODIFICATION received FDA 510(k) clearance on 1994-07-20, under 510(k) number K921294.

Who is the listed applicant for VIDEO ENDOSCOPE-RIGID MODIFICATION?

The FDA 510(k) record lists Medical Dynamics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIDEO ENDOSCOPE-RIGID MODIFICATION?

The FDA product code for VIDEO ENDOSCOPE-RIGID MODIFICATION is HET.

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Other records listing Medical Dynamics, Inc. as applicant

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K974542TRUE VISION, TRUE VISION IIK934682SURGICAL VIDEO CAMERA AND ACCESSORIESK930568ADAIR/VERESS NEEDLE INTRODUCER SETK915538OVER THE WIRE STONE BASKETK914315OPTICAL CATHETER INTRODUCER SETS, MODIFICATIONK913986CHOLANGIOGRAPHY/CHOLANGIOSCOPY/LIHOPAXY SYSTEM

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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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