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FDA 510(k)

ENDOMETRIAL SAMPLING SYRINGE

K-Number: K040189 · 2004-10-04

Decision Date2004-10-04
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ENDOMETRIAL SAMPLING SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Rocket Medical Plc. It received FDA 510(k) clearance on 2004-10-04 under 510(k) number K040189. 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 SAMPLING SYRINGE?

ENDOMETRIAL SAMPLING SYRINGE is a medical device that received FDA 510(k) clearance on 2004-10-04. The listed applicant is Rocket Medical Plc. The 510(k) number is K040189.

When did ENDOMETRIAL SAMPLING SYRINGE receive FDA 510(k) clearance?

ENDOMETRIAL SAMPLING SYRINGE received FDA 510(k) clearance on 2004-10-04, under 510(k) number K040189.

Who is the listed applicant for ENDOMETRIAL SAMPLING SYRINGE?

The FDA 510(k) record lists Rocket Medical Plc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOMETRIAL SAMPLING SYRINGE?

The FDA product code for ENDOMETRIAL SAMPLING SYRINGE 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 Rocket Medical Plc 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.

View all 19 devices →

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

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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