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)

MENICON SP VIAL

K-Number: K950878 · 1995-04-07

ApplicantHyman, Phelps & McNamara, P.C.
Decision Date1995-04-07
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MENICON SP VIAL is the device name listed in this FDA 510(k) record. The listed applicant is Hyman, Phelps & McNamara, P.C.. It received FDA 510(k) clearance on 1995-04-07 under 510(k) number K950878. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENICON SP VIAL?

MENICON SP VIAL is a medical device that received FDA 510(k) clearance on 1995-04-07. The listed applicant is Hyman, Phelps & McNamara, P.C.. The 510(k) number is K950878.

When did MENICON SP VIAL receive FDA 510(k) clearance?

MENICON SP VIAL received FDA 510(k) clearance on 1995-04-07, under 510(k) number K950878.

Who is the listed applicant for MENICON SP VIAL?

The FDA 510(k) record lists Hyman, Phelps & McNamara, P.C. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MENICON SP VIAL?

The FDA product code for MENICON SP VIAL is LRX.

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 Hyman, Phelps & McNamara, P.C. 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.

K950530PRO-TEC-CASEK945834PROPHY PRO.K915574COMFORT PERSONAL LUBRICANT

Related Devices (Code: LRX)

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.

K252175LANDR Contact LENS CaseFourth Axis, LLCK250495MINI VP1 (PL67_F); MINI VP1 (PL61_F)Avizor S.A.K240095CAREUS Contact Lens Case (Model 1, Model 2, Model 3, Model 4, Model 5, Model 6)Shanghai Care US Medical Product Co., Ltd.K231123Phoenix Contact Lens Case - dome top flat pack (CL-01); Phoenix Contact Lens Case - classic flat pack (CL-02); Phoenix Contact Lens Case - sunglass shape flat pack (CL-03)Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.K173538Clear Care Cleaning & Disinfecting Solution, AOCup Lens Case with AODiscAlcon Laboratories, Inc.K172925Contact Lens Case, Model: A-1, B-1P L Overseas Limited

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.

↑