Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CUP BIOPSY FORCEPS, CURVED UP

K-Number: K873506 · 1987-11-02

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

Device Summary

CUP BIOPSY FORCEPS, CURVED UP 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 K873506. 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 CUP BIOPSY FORCEPS, CURVED UP?

CUP BIOPSY FORCEPS, CURVED UP 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 K873506.

When did CUP BIOPSY FORCEPS, CURVED UP receive FDA 510(k) clearance?

CUP BIOPSY FORCEPS, CURVED UP received FDA 510(k) clearance on 1987-11-02, under 510(k) number K873506.

Who is the listed applicant for CUP BIOPSY FORCEPS, CURVED UP?

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 CUP BIOPSY FORCEPS, CURVED UP?

The FDA product code for CUP BIOPSY FORCEPS, CURVED UP 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑