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FDA 510(k)

CERVICAL BRUSH

K-Number: K884873 · 1989-02-09

ApplicantStatlab Medical Products, Inc.
Decision Date1989-02-09
Product CodeHHT
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CERVICAL BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Statlab Medical Products, Inc.. It received FDA 510(k) clearance on 1989-02-09 under 510(k) number K884873. 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 CERVICAL BRUSH?

CERVICAL BRUSH is a medical device that received FDA 510(k) clearance on 1989-02-09. The listed applicant is Statlab Medical Products, Inc.. The 510(k) number is K884873.

When did CERVICAL BRUSH receive FDA 510(k) clearance?

CERVICAL BRUSH received FDA 510(k) clearance on 1989-02-09, under 510(k) number K884873.

Who is the listed applicant for CERVICAL BRUSH?

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

What is the FDA product code for CERVICAL BRUSH?

The FDA product code for CERVICAL BRUSH is HHT.

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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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