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FDA 510(k)

SUTURE REMOVAL SET

K-Number: K770595 · 1977-05-23

ApplicantAbco Dealers, Inc.
Decision Date1977-05-23
Product CodeJOK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUTURE REMOVAL SET is the device name listed in this FDA 510(k) record. The listed applicant is Abco Dealers, Inc.. It received FDA 510(k) clearance on 1977-05-23 under 510(k) number K770595. The device is classified under product code JOK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUTURE REMOVAL SET?

SUTURE REMOVAL SET is a medical device that received FDA 510(k) clearance on 1977-05-23. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K770595.

When did SUTURE REMOVAL SET receive FDA 510(k) clearance?

SUTURE REMOVAL SET received FDA 510(k) clearance on 1977-05-23, under 510(k) number K770595.

Who is the listed applicant for SUTURE REMOVAL SET?

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

What is the FDA product code for SUTURE REMOVAL SET?

The FDA product code for SUTURE REMOVAL SET is JOK.

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Other records listing Abco Dealers, Inc. as applicant

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Related Devices (Code: JOK)

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.

K855131SUTURE REMOVAL KITDynarex Corp.K843075UTILITY SCISSORS DISPOSABLE ITEMSGreene International Corp.K812555DISPOSABLE SUTURE REMOVAL SCISSORSMedcare ProductsK770481SHEAR, PLASTIC HANDLE UTILITY S-475-7Acme United Corp.K770163SUTURE CUTTERConcept, Inc.K761192DRESSING CHANGE KITSuperior Plastic Products Corp.

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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