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FDA 510(k)

ESPI HOOK/UNIVERSAL SCISSORS, # 8101

K-Number: K903591 · 1990-09-12

Decision Date1990-09-12
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ESPI HOOK/UNIVERSAL SCISSORS, # 8101 is the device name listed in this FDA 510(k) record. The listed applicant is Dixon Medical, Inc.. It received FDA 510(k) clearance on 1990-09-12 under 510(k) number K903591. 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 ESPI HOOK/UNIVERSAL SCISSORS, # 8101?

ESPI HOOK/UNIVERSAL SCISSORS, # 8101 is a medical device that received FDA 510(k) clearance on 1990-09-12. The listed applicant is Dixon Medical, Inc.. The 510(k) number is K903591.

When did ESPI HOOK/UNIVERSAL SCISSORS, # 8101 receive FDA 510(k) clearance?

ESPI HOOK/UNIVERSAL SCISSORS, # 8101 received FDA 510(k) clearance on 1990-09-12, under 510(k) number K903591.

Who is the listed applicant for ESPI HOOK/UNIVERSAL SCISSORS, # 8101?

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

What is the FDA product code for ESPI HOOK/UNIVERSAL SCISSORS, # 8101?

The FDA product code for ESPI HOOK/UNIVERSAL SCISSORS, # 8101 is HET.

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 Dixon Medical, 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.

View all 12 devices →

Related Devices (Code: HET)

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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