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FDA 510(k)

PART #860070 ULTRAPAK & #860075 ULTRAPAK

K-Number: K871474 · 1987-08-10

Decision Date1987-08-10
Product CodeHOC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PART #860070 ULTRAPAK & #860075 ULTRAPAK is the device name listed in this FDA 510(k) record. The listed applicant is Medical Technical Products. It received FDA 510(k) clearance on 1987-08-10 under 510(k) number K871474. The device is classified under product code HOC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 8 devices →

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.

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