(DME) AUTO-MOD MODIFIED FOR AUTOCLAVING #D5280
K-Number: K870495 · 1987-03-30
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Device Summary
Frequently Asked Questions
What is the (DME) AUTO-MOD MODIFIED FOR AUTOCLAVING #D5280?
(DME) AUTO-MOD MODIFIED FOR AUTOCLAVING #D5280 is a medical device that received FDA 510(k) clearance on 1987-03-30. The listed applicant is Sigma Chemical Co.. The 510(k) number is K870495.
When did (DME) AUTO-MOD MODIFIED FOR AUTOCLAVING #D5280 receive FDA 510(k) clearance?
(DME) AUTO-MOD MODIFIED FOR AUTOCLAVING #D5280 received FDA 510(k) clearance on 1987-03-30, under 510(k) number K870495.
Who is the listed applicant for (DME) AUTO-MOD MODIFIED FOR AUTOCLAVING #D5280?
The FDA 510(k) record lists Sigma Chemical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for (DME) AUTO-MOD MODIFIED FOR AUTOCLAVING #D5280?
The FDA product code for (DME) AUTO-MOD MODIFIED FOR AUTOCLAVING #D5280 is KIT.
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 Sigma Chemical Co. 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: KIT)
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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