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FDA 510(k)

PAP SMEAR BRUSH

K-Number: K832986 · 1984-02-10

ApplicantDonald G. Zeller
Decision Date1984-02-10
Product CodeHHT
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PAP SMEAR BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Donald G. Zeller. It received FDA 510(k) clearance on 1984-02-10 under 510(k) number K832986. The device is classified under product code HHT. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAP SMEAR BRUSH?

PAP SMEAR BRUSH is a medical device that received FDA 510(k) clearance on 1984-02-10. The listed applicant is Donald G. Zeller. The 510(k) number is K832986.

When did PAP SMEAR BRUSH receive FDA 510(k) clearance?

PAP SMEAR BRUSH received FDA 510(k) clearance on 1984-02-10, under 510(k) number K832986.

Who is the listed applicant for PAP SMEAR BRUSH?

The FDA 510(k) record lists Donald G. Zeller as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PAP SMEAR BRUSH?

The FDA product code for PAP SMEAR BRUSH is HHT.

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

Related Devices (Code: HHT)

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.

K182049exCellerator Cervical Collection DeviceExcell Company, LLCK153128Kolplast Cervical Sample Collection KitKolplast CI SAK111681HISTOBRUSHPuritan Medical Products Company, LLCK083012PAPCONEOtto Bock Pur Life Science GmbHK081522BIO NUCLEAR DIAGNOSTICS (ENDO)CERVICAL SAMPLER FOR GYN CYTOLOGYBio Nuclear Diagnostics, Inc.K072381SOFTPAP CERVICAL CELL COLLECTORCytocore, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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