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FDA 510(k)

CERVICAL-VAGINAL SPATULA

K-Number: K761348 · 1977-01-18

Decision Date1977-01-18
Product CodeHHT
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CERVICAL-VAGINAL SPATULA is the device name listed in this FDA 510(k) record. The listed applicant is Law Offices of Natter & Natter. It received FDA 510(k) clearance on 1977-01-18 under 510(k) number K761348. The device is classified under product code HHT. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERVICAL-VAGINAL SPATULA?

CERVICAL-VAGINAL SPATULA is a medical device that received FDA 510(k) clearance on 1977-01-18. The listed applicant is Law Offices of Natter & Natter. The 510(k) number is K761348.

When did CERVICAL-VAGINAL SPATULA receive FDA 510(k) clearance?

CERVICAL-VAGINAL SPATULA received FDA 510(k) clearance on 1977-01-18, under 510(k) number K761348.

Who is the listed applicant for CERVICAL-VAGINAL SPATULA?

The FDA 510(k) record lists Law Offices of Natter & Natter as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CERVICAL-VAGINAL SPATULA?

The FDA product code for CERVICAL-VAGINAL SPATULA is HHT.

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.

Related Devices (Code: HHT)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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