WEED PULLER & PRUNER
K-Number: K761124 · 1976-12-02
Advertisement
Device Summary
Frequently Asked Questions
What is the WEED PULLER & PRUNER?
WEED PULLER & PRUNER is a medical device that received FDA 510(k) clearance on 1976-12-02. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K761124.
When did WEED PULLER & PRUNER receive FDA 510(k) clearance?
WEED PULLER & PRUNER received FDA 510(k) clearance on 1976-12-02, under 510(k) number K761124.
Who is the listed applicant for WEED PULLER & PRUNER?
The FDA 510(k) record lists Fred Sammons, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WEED PULLER & PRUNER?
The FDA product code for WEED PULLER & PRUNER is IKW.
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 Fred Sammons, 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.
Related Devices (Code: IKW)
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.
Advertisement