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FDA 510(k)

NEPHELOMETRIC SOLID TURBIDITY STANDARD

K-Number: K812220 · 1981-08-18

Decision Date1981-08-18
Product CodeJIW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NEPHELOMETRIC SOLID TURBIDITY STANDARD 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 1981-08-18 under 510(k) number K812220. The device is classified under product code JIW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEPHELOMETRIC SOLID TURBIDITY STANDARD?

NEPHELOMETRIC SOLID TURBIDITY STANDARD is a medical device that received FDA 510(k) clearance on 1981-08-18. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. The 510(k) number is K812220.

When did NEPHELOMETRIC SOLID TURBIDITY STANDARD receive FDA 510(k) clearance?

NEPHELOMETRIC SOLID TURBIDITY STANDARD received FDA 510(k) clearance on 1981-08-18, under 510(k) number K812220.

Who is the listed applicant for NEPHELOMETRIC SOLID TURBIDITY STANDARD?

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 NEPHELOMETRIC SOLID TURBIDITY STANDARD?

The FDA product code for NEPHELOMETRIC SOLID TURBIDITY STANDARD is JIW.

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: JIW)

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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