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FDA 510(k)

MASTERSON* ENDOMETRIAL BIOPSY KIT

K-Number: K791765 · 1979-11-05

ApplicantCodman & Shurtleff, Inc.
Decision Date1979-11-05
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MASTERSON* ENDOMETRIAL BIOPSY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1979-11-05 under 510(k) number K791765. 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 MASTERSON* ENDOMETRIAL BIOPSY KIT?

MASTERSON* ENDOMETRIAL BIOPSY KIT is a medical device that received FDA 510(k) clearance on 1979-11-05. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K791765.

When did MASTERSON* ENDOMETRIAL BIOPSY KIT receive FDA 510(k) clearance?

MASTERSON* ENDOMETRIAL BIOPSY KIT received FDA 510(k) clearance on 1979-11-05, under 510(k) number K791765.

Who is the listed applicant for MASTERSON* ENDOMETRIAL BIOPSY KIT?

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

What is the FDA product code for MASTERSON* ENDOMETRIAL BIOPSY KIT?

The FDA product code for MASTERSON* ENDOMETRIAL BIOPSY KIT is HHK.

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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.

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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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