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)

SUCTION ORA-SWAB(R) BRUSH KIT

K-Number: K901806 · 1990-08-15

ApplicantSage Products, Inc.
Decision Date1990-08-15
Product CodeEIA
Advisory CommitteeDE
DecisionUnknown

Device Summary

SUCTION ORA-SWAB(R) BRUSH KIT is the device name listed in this FDA 510(k) record. The listed applicant is Sage Products, Inc.. It received FDA 510(k) clearance on 1990-08-15 under 510(k) number K901806. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SUCTION ORA-SWAB(R) BRUSH KIT?

SUCTION ORA-SWAB(R) BRUSH KIT is a medical device that received FDA 510(k) clearance on 1990-08-15. The listed applicant is Sage Products, Inc.. The 510(k) number is K901806.

When did SUCTION ORA-SWAB(R) BRUSH KIT receive FDA 510(k) clearance?

SUCTION ORA-SWAB(R) BRUSH KIT received FDA 510(k) clearance on 1990-08-15, under 510(k) number K901806.

Who is the listed applicant for SUCTION ORA-SWAB(R) BRUSH KIT?

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

What is the FDA product code for SUCTION ORA-SWAB(R) BRUSH KIT?

The FDA product code for SUCTION ORA-SWAB(R) BRUSH KIT is EIA.

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 Sage Products, 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.

K972705RESHEATHER DEVICE-METAL OR PLASTIC, RESHEATER/ NEEDLE HOLDER DEVICE-PLASTICK980490SAGE PRODUCTS INC, SHARPS DISPOSAL CONTAINERS WITH SCREW TOP CAPSK9739112 GALLON ALTERNATE CARE SHARPS CONTAINERK972279SHARPS SHUTTLEK970135NITRILE GLOVESK972302POCKET COUNT OR SAFETCOUNT

View all 31 devices →

Related Devices (Code: EIA)

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.

K251544Dental Unit (MP2000-550LED-2.0, LP2100-550LED-2.0)Lakong Medical Devices Co., Ltd.K251626Midmark Dental Delivery SystemMidmark CorporationK251491K5 Cart, K5 Mount, K5 SwingOsstem Implant Company., Ltd. Chair BusinessK243130Integral Dental UnitGuangdong Yadeng Medical Apparatus Co., Ltd.,K242611Integral Dental UnitsMipont Medical Equipment Co., Ltd.K250473Dental Delivery System Series 5 and Dental Delivery System Series 5 PlusDci International, LLC

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.

↑