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FDA 510(k)

CYTO PAK PAP SMEAR KIT

K-Number: K923143 · 1993-07-16

Decision Date1993-07-16
Product CodeHHT
Advisory CommitteeOB
DecisionUnknown

Device Summary

CYTO PAK PAP SMEAR KIT is the device name listed in this FDA 510(k) record. The listed applicant is International Medical Equipment Brokers, Inc.. It received FDA 510(k) clearance on 1993-07-16 under 510(k) number K923143. The device is classified under product code HHT. It was reviewed by the OB advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CYTO PAK PAP SMEAR KIT?

CYTO PAK PAP SMEAR KIT is a medical device that received FDA 510(k) clearance on 1993-07-16. The listed applicant is International Medical Equipment Brokers, Inc.. The 510(k) number is K923143.

When did CYTO PAK PAP SMEAR KIT receive FDA 510(k) clearance?

CYTO PAK PAP SMEAR KIT received FDA 510(k) clearance on 1993-07-16, under 510(k) number K923143.

Who is the listed applicant for CYTO PAK PAP SMEAR KIT?

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

What is the FDA product code for CYTO PAK PAP SMEAR KIT?

The FDA product code for CYTO PAK PAP SMEAR KIT 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.

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.

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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