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FDA 510(k)

VACUUM RELIEF VALVE

K-Number: K760894 · 1976-12-09

ApplicantDelta Medical Industries
Decision Date1976-12-09
Product CodeDWD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VACUUM RELIEF VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Delta Medical Industries. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K760894. The device is classified under product code DWD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACUUM RELIEF VALVE?

VACUUM RELIEF VALVE is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Delta Medical Industries. The 510(k) number is K760894.

When did VACUUM RELIEF VALVE receive FDA 510(k) clearance?

VACUUM RELIEF VALVE received FDA 510(k) clearance on 1976-12-09, under 510(k) number K760894.

Who is the listed applicant for VACUUM RELIEF VALVE?

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

What is the FDA product code for VACUUM RELIEF VALVE?

The FDA product code for VACUUM RELIEF VALVE is DWD.

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Other records listing Delta Medical 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.

K833884ISOTEC DISPOS. PRESSURE TRANSDUCERK840253ONE-WAY AIR VALVEK832470INFUSION PUMPK830389ACCU-RYNGE PUMP SP-250K831750PM-3K822761DELIVERY TUBE SET #2226

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Related Devices (Code: DWD)

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.

K992657IBC VRV, MODEL 1350International Biophysics Corp.K920077NIKKISO NK PUMPInternational Medical Products, Inc.K915480B-D ULTRA-VUE PROCEDURE NEEDLE W/ SPINAL TYPE PT.Bd Becton Dickinson Vacutainer Systems PreanalyticK915481B-D ULTRA-VUE PROCEDURE NEEDLE W/ CHIBA TYPE POINTBd Becton Dickinson Vacutainer Systems PreanalyticK915482B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PTBd Becton Dickinson Vacutainer Systems PreanalyticK905311DURAFLO II HEPARIN TREATED SUCTION WANDS VAR. MOD.Baxter Bentley Laboratories, Inc.

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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