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FDA 510(k)

VIDEO ENDOSCOPE, RIGID

K-Number: K903339 · 1991-03-06

ApplicantMedical Dynamics, Inc.
Decision Date1991-03-06
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

VIDEO ENDOSCOPE, RIGID 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 1991-03-06 under 510(k) number K903339. 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?

VIDEO ENDOSCOPE, RIGID is a medical device that received FDA 510(k) clearance on 1991-03-06. The listed applicant is Medical Dynamics, Inc.. The 510(k) number is K903339.

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

VIDEO ENDOSCOPE, RIGID received FDA 510(k) clearance on 1991-03-06, under 510(k) number K903339.

Who is the listed applicant for VIDEO ENDOSCOPE, RIGID?

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?

The FDA product code for VIDEO ENDOSCOPE, RIGID is HET.

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Other records listing Medical Dynamics, 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.

K974542TRUE VISION, TRUE VISION IIK921294VIDEO ENDOSCOPE-RIGID MODIFICATIONK934682SURGICAL VIDEO CAMERA AND ACCESSORIESK930568ADAIR/VERESS NEEDLE INTRODUCER SETK915538OVER THE WIRE STONE BASKETK914315OPTICAL CATHETER INTRODUCER SETS, MODIFICATION

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Related Devices (Code: HET)

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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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