(D-PBS) MODIFIED HYBRI-MAX PRODUCT NO. D7030
K-Number: K870482 · 1987-03-30
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Device Summary
Frequently Asked Questions
What is the (D-PBS) MODIFIED HYBRI-MAX PRODUCT NO. D7030?
(D-PBS) MODIFIED HYBRI-MAX PRODUCT NO. D7030 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 K870482.
When did (D-PBS) MODIFIED HYBRI-MAX PRODUCT NO. D7030 receive FDA 510(k) clearance?
(D-PBS) MODIFIED HYBRI-MAX PRODUCT NO. D7030 received FDA 510(k) clearance on 1987-03-30, under 510(k) number K870482.
Who is the listed applicant for (D-PBS) MODIFIED HYBRI-MAX PRODUCT NO. D7030?
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 (D-PBS) MODIFIED HYBRI-MAX PRODUCT NO. D7030?
The FDA product code for (D-PBS) MODIFIED HYBRI-MAX PRODUCT NO. D7030 is KIP.
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: KIP)
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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