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)

UTERINE ASPIRATION CURETTES(RIGID&FLEX)

K-Number: K812426 · 1981-10-08

ApplicantMedi-Spec
Decision Date1981-10-08
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

UTERINE ASPIRATION CURETTES(RIGID&FLEX) is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Spec. It received FDA 510(k) clearance on 1981-10-08 under 510(k) number K812426. 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 UTERINE ASPIRATION CURETTES(RIGID&FLEX)?

UTERINE ASPIRATION CURETTES(RIGID&FLEX) is a medical device that received FDA 510(k) clearance on 1981-10-08. The listed applicant is Medi-Spec. The 510(k) number is K812426.

When did UTERINE ASPIRATION CURETTES(RIGID&FLEX) receive FDA 510(k) clearance?

UTERINE ASPIRATION CURETTES(RIGID&FLEX) received FDA 510(k) clearance on 1981-10-08, under 510(k) number K812426.

Who is the listed applicant for UTERINE ASPIRATION CURETTES(RIGID&FLEX)?

The FDA 510(k) record lists Medi-Spec as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UTERINE ASPIRATION CURETTES(RIGID&FLEX)?

The FDA product code for UTERINE ASPIRATION CURETTES(RIGID&FLEX) 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 Medi-Spec 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 8 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.

↑