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FDA 510(k)

KARICKHOFF FLYING CORPUSCLE VIEWER

K-Number: K831829 · 1983-10-19

Decision Date1983-10-19
Product CodeHIX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

KARICKHOFF FLYING CORPUSCLE VIEWER is the device name listed in this FDA 510(k) record. The listed applicant is Surgidev Corp.. It received FDA 510(k) clearance on 1983-10-19 under 510(k) number K831829. The device is classified under product code HIX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARICKHOFF FLYING CORPUSCLE VIEWER?

KARICKHOFF FLYING CORPUSCLE VIEWER is a medical device that received FDA 510(k) clearance on 1983-10-19. The listed applicant is Surgidev Corp.. The 510(k) number is K831829.

When did KARICKHOFF FLYING CORPUSCLE VIEWER receive FDA 510(k) clearance?

KARICKHOFF FLYING CORPUSCLE VIEWER received FDA 510(k) clearance on 1983-10-19, under 510(k) number K831829.

Who is the listed applicant for KARICKHOFF FLYING CORPUSCLE VIEWER?

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

What is the FDA product code for KARICKHOFF FLYING CORPUSCLE VIEWER?

The FDA product code for KARICKHOFF FLYING CORPUSCLE VIEWER is HIX.

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.

Other records listing Surgidev Corp. 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.

Related Devices (Code: HIX)

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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