PART #860070 ULTRAPAK & #860075 ULTRAPAK
K-Number: K871474 · 1987-08-10
Advertisement
Device Summary
Frequently Asked Questions
What is the PART #860070 ULTRAPAK & #860075 ULTRAPAK?
PART #860070 ULTRAPAK & #860075 ULTRAPAK is a medical device that received FDA 510(k) clearance on 1987-08-10. The listed applicant is Medical Technical Products. The 510(k) number is K871474.
When did PART #860070 ULTRAPAK & #860075 ULTRAPAK receive FDA 510(k) clearance?
PART #860070 ULTRAPAK & #860075 ULTRAPAK received FDA 510(k) clearance on 1987-08-10, under 510(k) number K871474.
Who is the listed applicant for PART #860070 ULTRAPAK & #860075 ULTRAPAK?
The FDA 510(k) record lists Medical Technical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PART #860070 ULTRAPAK & #860075 ULTRAPAK?
The FDA product code for PART #860070 ULTRAPAK & #860075 ULTRAPAK is HOC.
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 Technical Products 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: HOC)
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.
Advertisement