BIOPSY/MYELO/ARTHRO/AMNIOCENT/BASIC SKIN PREP TRAY
K-Number: K924958 · 1993-06-07
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Device Summary
Frequently Asked Questions
What is the BIOPSY/MYELO/ARTHRO/AMNIOCENT/BASIC SKIN PREP TRAY?
BIOPSY/MYELO/ARTHRO/AMNIOCENT/BASIC SKIN PREP TRAY is a medical device that received FDA 510(k) clearance on 1993-06-07. The listed applicant is Medical Insights, Inc.. The 510(k) number is K924958.
When did BIOPSY/MYELO/ARTHRO/AMNIOCENT/BASIC SKIN PREP TRAY receive FDA 510(k) clearance?
BIOPSY/MYELO/ARTHRO/AMNIOCENT/BASIC SKIN PREP TRAY received FDA 510(k) clearance on 1993-06-07, under 510(k) number K924958.
Who is the listed applicant for BIOPSY/MYELO/ARTHRO/AMNIOCENT/BASIC SKIN PREP TRAY?
The FDA 510(k) record lists Medical Insights, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOPSY/MYELO/ARTHRO/AMNIOCENT/BASIC SKIN PREP TRAY?
The FDA product code for BIOPSY/MYELO/ARTHRO/AMNIOCENT/BASIC SKIN PREP TRAY is KDD.
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 Medical Insights, 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: KDD)
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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