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FDA 510(k)

ENDOMETRIAL SAMPLER

K-Number: K872908 · 1987-10-20

ApplicantZinnanti Surgical Instruments, Inc.
Decision Date1987-10-20
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ENDOMETRIAL SAMPLER is the device name listed in this FDA 510(k) record. The listed applicant is Zinnanti Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1987-10-20 under 510(k) number K872908. 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 SAMPLER?

ENDOMETRIAL SAMPLER is a medical device that received FDA 510(k) clearance on 1987-10-20. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K872908.

When did ENDOMETRIAL SAMPLER receive FDA 510(k) clearance?

ENDOMETRIAL SAMPLER received FDA 510(k) clearance on 1987-10-20, under 510(k) number K872908.

Who is the listed applicant for ENDOMETRIAL SAMPLER?

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

What is the FDA product code for ENDOMETRIAL SAMPLER?

The FDA product code for ENDOMETRIAL SAMPLER is HHK.

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Other records listing Zinnanti Surgical Instruments, Inc. as applicant

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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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