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FDA 510(k)

ISOTEC DISPOS. PRESSURE TRANSDUCER

K-Number: K833884 · 1984-04-17

ApplicantDelta Medical Industries
Decision Date1984-04-17
Product Code
DecisionSubstantially Equivalent

Device Summary

ISOTEC DISPOS. PRESSURE TRANSDUCER 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 1984-04-17 under 510(k) number K833884. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ISOTEC DISPOS. PRESSURE TRANSDUCER?

ISOTEC DISPOS. PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is Delta Medical Industries. The 510(k) number is K833884.

When did ISOTEC DISPOS. PRESSURE TRANSDUCER receive FDA 510(k) clearance?

ISOTEC DISPOS. PRESSURE TRANSDUCER received FDA 510(k) clearance on 1984-04-17, under 510(k) number K833884.

Who is the listed applicant for ISOTEC DISPOS. PRESSURE TRANSDUCER?

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

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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.

K840253ONE-WAY AIR VALVEK832470INFUSION PUMPK830389ACCU-RYNGE PUMP SP-250K831750PM-3K822761DELIVERY TUBE SET #2226K820912PMS-2 PRESSURE MONITOR SEPARATOR

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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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