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)

ADSON FORCEPS 4 3/4

K-Number: K821284 · 1982-05-28

ApplicantConphar, Inc.
Decision Date1982-05-28
Product CodeEFL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ADSON FORCEPS 4 3/4 is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1982-05-28 under 510(k) number K821284. The device is classified under product code EFL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADSON FORCEPS 4 3/4?

ADSON FORCEPS 4 3/4 is a medical device that received FDA 510(k) clearance on 1982-05-28. The listed applicant is Conphar, Inc.. The 510(k) number is K821284.

When did ADSON FORCEPS 4 3/4 receive FDA 510(k) clearance?

ADSON FORCEPS 4 3/4 received FDA 510(k) clearance on 1982-05-28, under 510(k) number K821284.

Who is the listed applicant for ADSON FORCEPS 4 3/4?

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 ADSON FORCEPS 4 3/4?

The FDA product code for ADSON FORCEPS 4 3/4 is EFL.

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: EFL)

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.

K890243DRESSING FORCEPSKinetic Medical ProductsK821778BEACH DRESSING PLIERPacific Dental Corp.K821285SPLINTER FORCEPS 4 1/2Conphar, Inc.K821282THUMB DRESSING FORCEPS 5Conphar, 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.

↑