FDA 510(k)

MODEL 2500 PNEUMATIC PERCUSSOR

K-Number: K802399 · 1980-10-23

ApplicantMedical Equipment Development Co., Inc.

Decision Date1980-10-23

Product CodeBYI

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

MODEL 2500 PNEUMATIC PERCUSSOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Equipment Development Co., Inc.. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K802399. The device is classified under product code BYI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 2500 PNEUMATIC PERCUSSOR?

MODEL 2500 PNEUMATIC PERCUSSOR is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Medical Equipment Development Co., Inc.. The 510(k) number is K802399.

When did MODEL 2500 PNEUMATIC PERCUSSOR receive FDA 510(k) clearance?

MODEL 2500 PNEUMATIC PERCUSSOR received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802399.

Who is the listed applicant for MODEL 2500 PNEUMATIC PERCUSSOR?

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

What is the FDA product code for MODEL 2500 PNEUMATIC PERCUSSOR?

The FDA product code for MODEL 2500 PNEUMATIC PERCUSSOR is BYI.

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 Medical Equipment Development Co., Inc. as applicant

K911973LINEAR ACCELERATOR COLLIMATOR K901670GNOMOS STEREOTACTIC DEVICE K895537MODIFIED MEMORY RETRACTOR ARM K893911MED-TECH RADIOLUCENT HEAD FIXATION SYSTEM K874829MEDCO MEMORY RETRACTOR SYSTEM K874833ARC ADAPTER ASSEMBLY

View all 7 devices →

Related Devices (Code: BYI)

K252849AffloVest® Mobile Airway Clearance TherapyTactile Medical K250860BreatheBand® (Model 1000)Exemplar Medical, LLC K242063LibAirty Airway Clearance SystemSynchrony Medical , Ltd.K240959Respiratory Muscle TrainerChongqing Moffy Innovation Technology Co., Ltd.K233441The Vest APX System (PVAPX1)Baxter Healthcare Corportation K222496Electromed SmartVest Airway Clearance SystemElectromed, 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.