STERI-TRACTOR WOUND RETRACTOR
K-Number: K870543 · 1987-02-24
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Device Summary
Frequently Asked Questions
What is the STERI-TRACTOR WOUND RETRACTOR?
STERI-TRACTOR WOUND RETRACTOR is a medical device that received FDA 510(k) clearance on 1987-02-24. The listed applicant is 3M Company. The 510(k) number is K870543.
When did STERI-TRACTOR WOUND RETRACTOR receive FDA 510(k) clearance?
STERI-TRACTOR WOUND RETRACTOR received FDA 510(k) clearance on 1987-02-24, under 510(k) number K870543.
Who is the listed applicant for STERI-TRACTOR WOUND RETRACTOR?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERI-TRACTOR WOUND RETRACTOR?
The FDA product code for STERI-TRACTOR WOUND RETRACTOR is GAD.
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 3M Company 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: GAD)
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.
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