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FDA 510(k)

TMA BICARBONATE/GLYCEROL DILUENT

K-Number: K771700 · 1977-11-11

ApplicantHyland Therapeutic Div., Travenol Laboratories
Decision Date1977-11-11
Product Code
DecisionSubstantially Equivalent

Device Summary

TMA BICARBONATE/GLYCEROL DILUENT 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 1977-11-11 under 510(k) number K771700. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TMA BICARBONATE/GLYCEROL DILUENT?

TMA BICARBONATE/GLYCEROL DILUENT is a medical device that received FDA 510(k) clearance on 1977-11-11. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. The 510(k) number is K771700.

When did TMA BICARBONATE/GLYCEROL DILUENT receive FDA 510(k) clearance?

TMA BICARBONATE/GLYCEROL DILUENT received FDA 510(k) clearance on 1977-11-11, under 510(k) number K771700.

Who is the listed applicant for TMA BICARBONATE/GLYCEROL DILUENT?

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

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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.

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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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