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FDA 510(k)

SERRATED GRASPING FORCEPS, CURVED DOWN

K-Number: K873510 · 1987-11-02

Decision Date1987-11-02
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SERRATED GRASPING FORCEPS, CURVED DOWN is the device name listed in this FDA 510(k) record. The listed applicant is Arthropedics, Inc.. It received FDA 510(k) clearance on 1987-11-02 under 510(k) number K873510. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERRATED GRASPING FORCEPS, CURVED DOWN?

SERRATED GRASPING FORCEPS, CURVED DOWN is a medical device that received FDA 510(k) clearance on 1987-11-02. The listed applicant is Arthropedics, Inc.. The 510(k) number is K873510.

When did SERRATED GRASPING FORCEPS, CURVED DOWN receive FDA 510(k) clearance?

SERRATED GRASPING FORCEPS, CURVED DOWN received FDA 510(k) clearance on 1987-11-02, under 510(k) number K873510.

Who is the listed applicant for SERRATED GRASPING FORCEPS, CURVED DOWN?

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

What is the FDA product code for SERRATED GRASPING FORCEPS, CURVED DOWN?

The FDA product code for SERRATED GRASPING FORCEPS, CURVED DOWN is HTD.

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 Arthropedics, 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.

View all 29 devices →

Related Devices (Code: HTD)

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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