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FDA 510(k)

BLOOD/FLUID WARMER MODEL DW-1000A

K-Number: K770232 · 1977-02-14

ApplicantGorman Rupp Industries
Decision Date1977-02-14
Product CodeBSB
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

BLOOD/FLUID WARMER MODEL DW-1000A is the device name listed in this FDA 510(k) record. The listed applicant is Gorman Rupp Industries. It received FDA 510(k) clearance on 1977-02-14 under 510(k) number K770232. The device is classified under product code BSB. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD/FLUID WARMER MODEL DW-1000A?

BLOOD/FLUID WARMER MODEL DW-1000A is a medical device that received FDA 510(k) clearance on 1977-02-14. The listed applicant is Gorman Rupp Industries. The 510(k) number is K770232.

When did BLOOD/FLUID WARMER MODEL DW-1000A receive FDA 510(k) clearance?

BLOOD/FLUID WARMER MODEL DW-1000A received FDA 510(k) clearance on 1977-02-14, under 510(k) number K770232.

Who is the listed applicant for BLOOD/FLUID WARMER MODEL DW-1000A?

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

What is the FDA product code for BLOOD/FLUID WARMER MODEL DW-1000A?

The FDA product code for BLOOD/FLUID WARMER MODEL DW-1000A is BSB.

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.

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Other records listing Gorman Rupp Industries 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.

K771537AQUAMATIC K-MODULE MODEL K-20K770839AQUAMATIC K-77K761337AQUAMATIC K-MODULE MODEL K-10K760910DISPOSABLE K-PADSK761087ELECTRONIC CONTROL UNIT

Related Devices (Code: BSB)

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.

K112639THE BELMONT BUDDY LITE FLUID WARMERBelmont Instrument Corp.K090508THE BELMONT BUDDY LITE FLUID WARMERBelmont Instrument Corp.K062774BELMONT BUDDY PLUS FLUID WARMERBelmont Instrument Corp.K052547BELMONT BUDDY FLUID WARMERBelmont Instrument Corp.K031478MICROHEATERBelmont Instrument Corp.K020060ASTOFLONats Corp.

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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