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)

THE STRIPPER PGD

K-Number: K041435 · 2004-09-29

ApplicantMid-Atlantic Diagnostics, Inc.
Decision Date2004-09-29
Product CodeMQH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

THE STRIPPER PGD is the device name listed in this FDA 510(k) record. The listed applicant is Mid-Atlantic Diagnostics, Inc.. It received FDA 510(k) clearance on 2004-09-29 under 510(k) number K041435. The device is classified under product code MQH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE STRIPPER PGD?

THE STRIPPER PGD is a medical device that received FDA 510(k) clearance on 2004-09-29. The listed applicant is Mid-Atlantic Diagnostics, Inc.. The 510(k) number is K041435.

When did THE STRIPPER PGD receive FDA 510(k) clearance?

THE STRIPPER PGD received FDA 510(k) clearance on 2004-09-29, under 510(k) number K041435.

Who is the listed applicant for THE STRIPPER PGD?

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

What is the FDA product code for THE STRIPPER PGD?

The FDA product code for THE STRIPPER PGD is MQH.

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 Mid-Atlantic Diagnostics, 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.

K100596CRYOPETTEK030525CUSTOM PRODUCTS IVF WORKSTATION TYPE WKST-24*36, WKST-24*48, WKST-24*60, WKST-24*72 AND WKST-24*72D PLUS ACCESSORIESK993699THE STRIPPER

Related Devices (Code: MQH)

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.

K250838Denudation PipettesGuangzhou Pinzhi Medical Device Co., Ltd.K192146V-DENUPETVitromed GmbHK161275EZ-Tip Singles, EZ-Tip Vial of 20, EZ-GripResearch Instruments LimitedK152581LifeGlobal Micro TipsLife Global Group, LLCK151018Embryo Biopsy Pipette, Polar Body Biopsy Pipette, Testicular Sperm Extraction PipetteCook IncorporatedK102480INJECTION PIPETTE; HOLDING PIPETTE; BIOPSY PIPETTE; DENUDING PIPETTE; PARTIAL ZONA DISSECTION (PZD) PIPETTE; ASSISTED HAJieying Laboratory, 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.

↑