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FDA 510(k)

ASPIRATOR & PROBE, CYTOLOGY, ENDOMET.

K-Number: K772121 · 1977-11-17

ApplicantSmithkline Diagnostics, Inc.
Decision Date1977-11-17
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ASPIRATOR & PROBE, CYTOLOGY, ENDOMET. is the device name listed in this FDA 510(k) record. The listed applicant is Smithkline Diagnostics, Inc.. It received FDA 510(k) clearance on 1977-11-17 under 510(k) number K772121. The device is classified under product code HHK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASPIRATOR & PROBE, CYTOLOGY, ENDOMET.?

ASPIRATOR & PROBE, CYTOLOGY, ENDOMET. is a medical device that received FDA 510(k) clearance on 1977-11-17. The listed applicant is Smithkline Diagnostics, Inc.. The 510(k) number is K772121.

When did ASPIRATOR & PROBE, CYTOLOGY, ENDOMET. receive FDA 510(k) clearance?

ASPIRATOR & PROBE, CYTOLOGY, ENDOMET. received FDA 510(k) clearance on 1977-11-17, under 510(k) number K772121.

Who is the listed applicant for ASPIRATOR & PROBE, CYTOLOGY, ENDOMET.?

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

What is the FDA product code for ASPIRATOR & PROBE, CYTOLOGY, ENDOMET.?

The FDA product code for ASPIRATOR & PROBE, CYTOLOGY, ENDOMET. is HHK.

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Related Devices (Code: HHK)

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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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