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FDA 510(k)

CERVICAL CYTOLOGY C-BRUSH MODEL CMB-1010

K-Number: K980356 · 1998-04-16

ApplicantCanadian Medical Brush, Inc.
Decision Date1998-04-16
Product CodeHHT
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CERVICAL CYTOLOGY C-BRUSH MODEL CMB-1010 is the device name listed in this FDA 510(k) record. The listed applicant is Canadian Medical Brush, Inc.. It received FDA 510(k) clearance on 1998-04-16 under 510(k) number K980356. 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 CYTOLOGY C-BRUSH MODEL CMB-1010?

CERVICAL CYTOLOGY C-BRUSH MODEL CMB-1010 is a medical device that received FDA 510(k) clearance on 1998-04-16. The listed applicant is Canadian Medical Brush, Inc.. The 510(k) number is K980356.

When did CERVICAL CYTOLOGY C-BRUSH MODEL CMB-1010 receive FDA 510(k) clearance?

CERVICAL CYTOLOGY C-BRUSH MODEL CMB-1010 received FDA 510(k) clearance on 1998-04-16, under 510(k) number K980356.

Who is the listed applicant for CERVICAL CYTOLOGY C-BRUSH MODEL CMB-1010?

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

What is the FDA product code for CERVICAL CYTOLOGY C-BRUSH MODEL CMB-1010?

The FDA product code for CERVICAL CYTOLOGY C-BRUSH MODEL CMB-1010 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.

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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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