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FDA 510(k)

ORTHOPEDIC WOUND DRAINAGE SET WITH TROCAR

K-Number: K893394 · 1989-10-19

Decision Date1989-10-19
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ORTHOPEDIC WOUND DRAINAGE SET WITH TROCAR is the device name listed in this FDA 510(k) record. The listed applicant is Haemonetics Corp.. It received FDA 510(k) clearance on 1989-10-19 under 510(k) number K893394. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOPEDIC WOUND DRAINAGE SET WITH TROCAR?

ORTHOPEDIC WOUND DRAINAGE SET WITH TROCAR is a medical device that received FDA 510(k) clearance on 1989-10-19. The listed applicant is Haemonetics Corp.. The 510(k) number is K893394.

When did ORTHOPEDIC WOUND DRAINAGE SET WITH TROCAR receive FDA 510(k) clearance?

ORTHOPEDIC WOUND DRAINAGE SET WITH TROCAR received FDA 510(k) clearance on 1989-10-19, under 510(k) number K893394.

Who is the listed applicant for ORTHOPEDIC WOUND DRAINAGE SET WITH TROCAR?

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

What is the FDA product code for ORTHOPEDIC WOUND DRAINAGE SET WITH TROCAR?

The FDA product code for ORTHOPEDIC WOUND DRAINAGE SET WITH TROCAR is CAC.

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 Haemonetics 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.

View all 28 devices →

Related Devices (Code: CAC)

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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