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)

CONPHAR SCISSORS 4&1/2 SHARP BLUNT

K-Number: K821112 · 1982-05-07

ApplicantConphar, Inc.
Decision Date1982-05-07
Product CodeFZT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONPHAR SCISSORS 4&1/2 SHARP BLUNT is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1982-05-07 under 510(k) number K821112. The device is classified under product code FZT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONPHAR SCISSORS 4&1/2 SHARP BLUNT?

CONPHAR SCISSORS 4&1/2 SHARP BLUNT is a medical device that received FDA 510(k) clearance on 1982-05-07. The listed applicant is Conphar, Inc.. The 510(k) number is K821112.

When did CONPHAR SCISSORS 4&1/2 SHARP BLUNT receive FDA 510(k) clearance?

CONPHAR SCISSORS 4&1/2 SHARP BLUNT received FDA 510(k) clearance on 1982-05-07, under 510(k) number K821112.

Who is the listed applicant for CONPHAR SCISSORS 4&1/2 SHARP BLUNT?

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

What is the FDA product code for CONPHAR SCISSORS 4&1/2 SHARP BLUNT?

The FDA product code for CONPHAR SCISSORS 4&1/2 SHARP BLUNT is FZT.

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 Conphar, 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.

K821825CONPHAR SILICONE FEEDING TUBEK821295OLSEN HEGAR NEEDLE HOLDERSK821289MAYO-HEGAR NEEDLE HOLDERK821354CONPHAR MAYO HEGAR NEEDLE HOLDERK821298BACKHAUS CLAMP, 3 1/2K821290LITTAUER SCISSORS 5 1/2

View all 122 devices →

Related Devices (Code: FZT)

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.

K112400SMARTSHEARSNuscience Consulting and Management Group, LLCK890818AUTO SUTURE DISPOSABLE SURGICAL TROCAR*United States Surgical, A Division of Tyco HealthcK872990MICRINS SURGICAL SCISSORMicrins Surgical, Inc.K841741SINGLE HAIR TRANSPLANT GRAFTParis Products, Inc.K841247SPC DISPOSABLE CUTTERSurgical Products Corp.K822448SCISSORS, VARIOUSJ. Sklar Mfg. Co., 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.

↑