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FDA 510(k)

BLOOD BANK DRI-BATH

K-Number: K760928 · 1977-01-10

ApplicantThermolyne Corp.
Decision Date1977-01-10
Product CodeJTQ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BLOOD BANK DRI-BATH is the device name listed in this FDA 510(k) record. The listed applicant is Thermolyne Corp.. It received FDA 510(k) clearance on 1977-01-10 under 510(k) number K760928. The device is classified under product code JTQ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD BANK DRI-BATH?

BLOOD BANK DRI-BATH is a medical device that received FDA 510(k) clearance on 1977-01-10. The listed applicant is Thermolyne Corp.. The 510(k) number is K760928.

When did BLOOD BANK DRI-BATH receive FDA 510(k) clearance?

BLOOD BANK DRI-BATH received FDA 510(k) clearance on 1977-01-10, under 510(k) number K760928.

Who is the listed applicant for BLOOD BANK DRI-BATH?

The FDA 510(k) record lists Thermolyne Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOOD BANK DRI-BATH?

The FDA product code for BLOOD BANK DRI-BATH is JTQ.

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Other records listing Thermolyne Corp. 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.

K792095HISTO-CENTER IIK771617SPECI-MIXK770914INCUBATOR, PORTABLE, ACT-STAT

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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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