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FDA 510(k)

ENDOMETRIAL ASPIRATION BIOSPY KIT 182341

K-Number: K771149 · 1977-07-27

Decision Date1977-07-27
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ENDOMETRIAL ASPIRATION BIOSPY KIT 182341 is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1977-07-27 under 510(k) number K771149. 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 ENDOMETRIAL ASPIRATION BIOSPY KIT 182341?

ENDOMETRIAL ASPIRATION BIOSPY KIT 182341 is a medical device that received FDA 510(k) clearance on 1977-07-27. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K771149.

When did ENDOMETRIAL ASPIRATION BIOSPY KIT 182341 receive FDA 510(k) clearance?

ENDOMETRIAL ASPIRATION BIOSPY KIT 182341 received FDA 510(k) clearance on 1977-07-27, under 510(k) number K771149.

Who is the listed applicant for ENDOMETRIAL ASPIRATION BIOSPY KIT 182341?

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

What is the FDA product code for ENDOMETRIAL ASPIRATION BIOSPY KIT 182341?

The FDA product code for ENDOMETRIAL ASPIRATION BIOSPY KIT 182341 is HHK.

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.

Other records listing C.R. Bard, Inc. 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.

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Related Devices (Code: HHK)

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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