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FDA 510(k)

SURGICAL VIDEO CAMERA, MODEL 9500

K-Number: K902359 · 1990-07-12

Decision Date1990-07-12
Product CodeFWB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL VIDEO CAMERA, MODEL 9500 is the device name listed in this FDA 510(k) record. The listed applicant is Seitz Technical Products, Inc.. It received FDA 510(k) clearance on 1990-07-12 under 510(k) number K902359. The device is classified under product code FWB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL VIDEO CAMERA, MODEL 9500?

SURGICAL VIDEO CAMERA, MODEL 9500 is a medical device that received FDA 510(k) clearance on 1990-07-12. The listed applicant is Seitz Technical Products, Inc.. The 510(k) number is K902359.

When did SURGICAL VIDEO CAMERA, MODEL 9500 receive FDA 510(k) clearance?

SURGICAL VIDEO CAMERA, MODEL 9500 received FDA 510(k) clearance on 1990-07-12, under 510(k) number K902359.

Who is the listed applicant for SURGICAL VIDEO CAMERA, MODEL 9500?

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

What is the FDA product code for SURGICAL VIDEO CAMERA, MODEL 9500?

The FDA product code for SURGICAL VIDEO CAMERA, MODEL 9500 is FWB.

Related Clinical Trials

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.

Related Devices (Code: FWB)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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