ACE BRAND INSTANT COLD PACK
K-Number: K820282 · 1982-02-12
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Device Summary
Frequently Asked Questions
What is the ACE BRAND INSTANT COLD PACK?
ACE BRAND INSTANT COLD PACK is a medical device that received FDA 510(k) clearance on 1982-02-12. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K820282.
When did ACE BRAND INSTANT COLD PACK receive FDA 510(k) clearance?
ACE BRAND INSTANT COLD PACK received FDA 510(k) clearance on 1982-02-12, under 510(k) number K820282.
Who is the listed applicant for ACE BRAND INSTANT COLD PACK?
The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACE BRAND INSTANT COLD PACK?
The FDA product code for ACE BRAND INSTANT COLD PACK is IMD.
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 Bd Becton Dickinson Vacutainer Systems Preanalytic 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: IMD)
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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