Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SURGICAL INSTRUMENTS

K-Number: K801292 · 1980-06-20

Decision Date1980-06-20
Product Code
DecisionSubstantially Equivalent

Device Summary

SURGICAL INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is William Skidmore & Co., Ltd.. It received FDA 510(k) clearance on 1980-06-20 under 510(k) number K801292. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL INSTRUMENTS?

SURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1980-06-20. The listed applicant is William Skidmore & Co., Ltd.. The 510(k) number is K801292.

When did SURGICAL INSTRUMENTS receive FDA 510(k) clearance?

SURGICAL INSTRUMENTS received FDA 510(k) clearance on 1980-06-20, under 510(k) number K801292.

Who is the listed applicant for SURGICAL INSTRUMENTS?

The FDA 510(k) record lists William Skidmore & Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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.

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.

↑