Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES

K-Number: K801070 · 1980-07-21

ApplicantSherwood Medical Industries
Decision Date1980-07-21
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1980-07-21 under 510(k) number K801070. 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 SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES?

SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES is a medical device that received FDA 510(k) clearance on 1980-07-21. The listed applicant is Sherwood Medical Industries. The 510(k) number is K801070.

When did SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES receive FDA 510(k) clearance?

SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES received FDA 510(k) clearance on 1980-07-21, under 510(k) number K801070.

Who is the listed applicant for SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES?

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

What is the FDA product code for SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES?

The FDA product code for SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Sherwood Medical Industries 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.

K801071LANCER GLUCOSE RATE REAGENT KITK792013LANCER L-INA HUMAN REFERENCE SERUMK792014LANCER L-INA BUFFER, POLYMER, WASH SOLUK782077LANCER ICE CUBEK790523ARGYLE ESOPHAGEAL STETHOSCOPEK790196MONOJECT ARTERIAL BLOOD SAMPLING DEVICE

View all 62 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.

K251882Uterine Aspiration SetGcmedica Enterprise Ltd.(Wuxi)K240434RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)Li Medical Corporation , Ltd.K201952CrossGlide ETS PlusCrossbay MedicalK192534CrossBay Endometrial Tissue Sampler (ETS)Crossbay MedicalK102847DISPOSABLE ENDOMETRIAL SUCTION CURETTEJiangsu Suyun Medical Materials Co., Ltd.K092982THE PANPAC SUCTION CURETTEPanpac Medical Corporation

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.

↑