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)

SCISSOR, LEFT

K-Number: K873501 · 1987-11-02

ApplicantArthropedics, Inc.
Decision Date1987-11-02
Product CodeHRR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SCISSOR, LEFT 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 K873501. The device is classified under product code HRR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCISSOR, LEFT?

SCISSOR, LEFT 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 K873501.

When did SCISSOR, LEFT receive FDA 510(k) clearance?

SCISSOR, LEFT received FDA 510(k) clearance on 1987-11-02, under 510(k) number K873501.

Who is the listed applicant for SCISSOR, LEFT?

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 SCISSOR, LEFT?

The FDA product code for SCISSOR, LEFT is HRR.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K873619ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS)K873653MONOPOLAR CAUTERY BLADE TIP #TM-1701K873654MONOPOLAR CAUTERY CONICAL TIP #TM-1702K873655MONOPOLAR CAUTERY RETROGADE TIP #TM-1703K873387VIDEO ARTHROSCOPE, 1.7MM X 55 MMK873711RETROGRADE KNIFE, DISPOSABLE #TM-1613

View all 29 devices →

Related Devices (Code: HRR)

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.

K890261TRIGEMINAL SCISSORSKinetic Medical ProductsK890225SURGICAL SCISSORSKinetic Medical ProductsK890212MICROSURGICAL SCISSORSKinetic Medical ProductsK873502SCISSOR, RIGHTArthropedics, Inc.K85180069-100 TO 69-114 VARIOUS CUTICLE SCISSORSArtiberiaK842953ALL-HANDS MEDICAL SUPPLY SUTURE REMOVALAll-Hands Medical Supply, Inc.

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.

↑