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FDA 510(k)

Q-PAK CHEMISTRY RADIORECEPTOR CONTROL A

K-Number: K770010 · 1977-04-18

Decision Date1977-04-18
Product CodeJIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

Q-PAK CHEMISTRY RADIORECEPTOR CONTROL A is the device name listed in this FDA 510(k) record. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. It received FDA 510(k) clearance on 1977-04-18 under 510(k) number K770010. The device is classified under product code JIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Q-PAK CHEMISTRY RADIORECEPTOR CONTROL A?

Q-PAK CHEMISTRY RADIORECEPTOR CONTROL A is a medical device that received FDA 510(k) clearance on 1977-04-18. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. The 510(k) number is K770010.

When did Q-PAK CHEMISTRY RADIORECEPTOR CONTROL A receive FDA 510(k) clearance?

Q-PAK CHEMISTRY RADIORECEPTOR CONTROL A received FDA 510(k) clearance on 1977-04-18, under 510(k) number K770010.

Who is the listed applicant for Q-PAK CHEMISTRY RADIORECEPTOR CONTROL A?

The FDA 510(k) record lists Hyland Therapeutic Div., Travenol Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Q-PAK CHEMISTRY RADIORECEPTOR CONTROL A?

The FDA product code for Q-PAK CHEMISTRY RADIORECEPTOR CONTROL A is JIX.

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 Hyland Therapeutic Div., Travenol Laboratories 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 44 devices →

Related Devices (Code: JIX)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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