FDA 510(k)

SCISSORS

K-Number: K823651 · 1983-02-03

Decision Date1983-02-03

Product Code

DecisionSubstantially Equivalent

Device Summary

SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1983-02-03 under 510(k) number K823651. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCISSORS?

SCISSORS is a medical device that received FDA 510(k) clearance on 1983-02-03. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K823651.

When did SCISSORS receive FDA 510(k) clearance?

SCISSORS received FDA 510(k) clearance on 1983-02-03, under 510(k) number K823651.

Who is the listed applicant for SCISSORS?

The FDA 510(k) record lists Fred Sammons, 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Fred Sammons, Inc. as applicant

K880644ULTRA-PAN FOR ORTHOTIC PLASTICS (7262)K880647ADULT PERCEPTUAL MOTOR PUZZLES (5331-01)K831549ARM SLINGS K831548SPLINTS K831550FINGER BONIOMETER BK7506 K831544DELUXE TRACTION EXERCISE GLOVE BK5035

View all 278 devices →

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.