BONE BIOPSY SET
K-Number: K820293 · 1982-03-01
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Device Summary
Frequently Asked Questions
What is the BONE BIOPSY SET?
BONE BIOPSY SET is a medical device that received FDA 510(k) clearance on 1982-03-01. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K820293.
When did BONE BIOPSY SET receive FDA 510(k) clearance?
BONE BIOPSY SET received FDA 510(k) clearance on 1982-03-01, under 510(k) number K820293.
Who is the listed applicant for BONE BIOPSY SET?
The FDA 510(k) record lists The Anspach Effort, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BONE BIOPSY SET?
The FDA product code for BONE BIOPSY SET is KNW.
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 The Anspach Effort, 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: KNW)
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.
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