ABCO SUTURE REMOVAL KITS-METAL & PLASTIC FORCEPS
K-Number: K851313 · 1985-05-01
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Device Summary
Frequently Asked Questions
What is the ABCO SUTURE REMOVAL KITS-METAL & PLASTIC FORCEPS?
ABCO SUTURE REMOVAL KITS-METAL & PLASTIC FORCEPS is a medical device that received FDA 510(k) clearance on 1985-05-01. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K851313.
When did ABCO SUTURE REMOVAL KITS-METAL & PLASTIC FORCEPS receive FDA 510(k) clearance?
ABCO SUTURE REMOVAL KITS-METAL & PLASTIC FORCEPS received FDA 510(k) clearance on 1985-05-01, under 510(k) number K851313.
Who is the listed applicant for ABCO SUTURE REMOVAL KITS-METAL & PLASTIC FORCEPS?
The FDA 510(k) record lists Abco Dealers, Inc. 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.
Other records listing Abco Dealers, 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.
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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