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)

COTTLE LOWER LATERAL FORCEPS

K-Number: K772398 · 1978-01-17

Decision Date1978-01-17
Product CodeKAE
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

COTTLE LOWER LATERAL FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1978-01-17 under 510(k) number K772398. The device is classified under product code KAE. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COTTLE LOWER LATERAL FORCEPS?

COTTLE LOWER LATERAL FORCEPS is a medical device that received FDA 510(k) clearance on 1978-01-17. The listed applicant is Edward Weck, Inc.. The 510(k) number is K772398.

When did COTTLE LOWER LATERAL FORCEPS receive FDA 510(k) clearance?

COTTLE LOWER LATERAL FORCEPS received FDA 510(k) clearance on 1978-01-17, under 510(k) number K772398.

Who is the listed applicant for COTTLE LOWER LATERAL FORCEPS?

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

What is the FDA product code for COTTLE LOWER LATERAL FORCEPS?

The FDA product code for COTTLE LOWER LATERAL FORCEPS is KAE.

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 Edward Weck, Inc. 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 140 devices →

Related Devices (Code: KAE)

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.

↑