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)

CELL-MATE(TM) MASS CYTOLOGY-CELLULAR RETRIEVAL SYST

K-Number: K934193 · 1993-11-19

ApplicantBiosearch Medical Products, Inc.
Decision Date1993-11-19
Product CodeEOX
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CELL-MATE(TM) MASS CYTOLOGY-CELLULAR RETRIEVAL SYST is the device name listed in this FDA 510(k) record. The listed applicant is Biosearch Medical Products, Inc.. It received FDA 510(k) clearance on 1993-11-19 under 510(k) number K934193. The device is classified under product code EOX. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CELL-MATE(TM) MASS CYTOLOGY-CELLULAR RETRIEVAL SYST?

CELL-MATE(TM) MASS CYTOLOGY-CELLULAR RETRIEVAL SYST is a medical device that received FDA 510(k) clearance on 1993-11-19. The listed applicant is Biosearch Medical Products, Inc.. The 510(k) number is K934193.

When did CELL-MATE(TM) MASS CYTOLOGY-CELLULAR RETRIEVAL SYST receive FDA 510(k) clearance?

CELL-MATE(TM) MASS CYTOLOGY-CELLULAR RETRIEVAL SYST received FDA 510(k) clearance on 1993-11-19, under 510(k) number K934193.

Who is the listed applicant for CELL-MATE(TM) MASS CYTOLOGY-CELLULAR RETRIEVAL SYST?

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

What is the FDA product code for CELL-MATE(TM) MASS CYTOLOGY-CELLULAR RETRIEVAL SYST?

The FDA product code for CELL-MATE(TM) MASS CYTOLOGY-CELLULAR RETRIEVAL SYST is EOX.

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 Biosearch Medical 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.

K051480ENTERAL FEEDING TUBEK970145PERINEOMETER & VAGINAL PROBE (BIOFEEDBACK MONITOR #20 AND VAGINAL PROBE)K964871BIOSEARCH SYRING FLUSHING/CLEANING PUMP FOR BIOSEARCH ENDOSCOPIC INSTRUMENTSK951260URINARY INTERMITTENT CATHETERS W/O HYDROMER HYDROPHILIC LUBRICANTK944614MEGA-BRUSH, ENDOSCOPIC MASS CYTOLOGY - CELLUAR RETRIEVAL SYSTEMK932295NON-BALLOON REPLACEMENT GASTROSTOMY KIT

View all 70 devices →

Related Devices (Code: EOX)

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.

K233142EndoSign® Cell collection device (ES-CYT-102)Cyted LimitedK230339EsoCheck Cell Collection DeviceLucid Diagnostics, Inc.K223072PENTAX Medical Video Esophagoscope EE17-J10Pentax of America, Inc.K222366EsoCheck Cell Collection DeviceLucid Diagnostics, Inc.K203450EsophaCap Swallowable Cellular Retrieval Device (changed from Cell-Mata)Capnostics, LLCK210137EsoCheck Cell Collection DeviceLucid Diagnostics, 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.

↑