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FDA 510(k)

CYTOBRUSH

K-Number: K890706 · 1989-04-25

ApplicantLaboratoire Ccd C/O Washington Regulatory Services
Decision Date1989-04-25
Product CodeHHT
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CYTOBRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Laboratoire Ccd C/O Washington Regulatory Services. It received FDA 510(k) clearance on 1989-04-25 under 510(k) number K890706. 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 CYTOBRUSH?

CYTOBRUSH is a medical device that received FDA 510(k) clearance on 1989-04-25. The listed applicant is Laboratoire Ccd C/O Washington Regulatory Services. The 510(k) number is K890706.

When did CYTOBRUSH receive FDA 510(k) clearance?

CYTOBRUSH received FDA 510(k) clearance on 1989-04-25, under 510(k) number K890706.

Who is the listed applicant for CYTOBRUSH?

The FDA 510(k) record lists Laboratoire Ccd C/O Washington Regulatory Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CYTOBRUSH?

The FDA product code for CYTOBRUSH 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.

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Other records listing Laboratoire Ccd C/O Washington Regulatory Services 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.

K884696RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SETK881456PIPELLE DE CORNIER ENDOMETRIAL SUCTION CURETTEK881220ENDOCYTE, DISPOSABLE ENDOMETRIAL SAMPLER

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

View on FDA Database →

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

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