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FDA 510(k)

TEMP. SENSOR W/22MM FITTINGS

K-Number: K780260 · 1978-03-14

Decision Date1978-03-14
Product CodeKPD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TEMP. SENSOR W/22MM FITTINGS is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1978-03-14 under 510(k) number K780260. The device is classified under product code KPD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMP. SENSOR W/22MM FITTINGS?

TEMP. SENSOR W/22MM FITTINGS is a medical device that received FDA 510(k) clearance on 1978-03-14. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K780260.

When did TEMP. SENSOR W/22MM FITTINGS receive FDA 510(k) clearance?

TEMP. SENSOR W/22MM FITTINGS received FDA 510(k) clearance on 1978-03-14, under 510(k) number K780260.

Who is the listed applicant for TEMP. SENSOR W/22MM FITTINGS?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEMP. SENSOR W/22MM FITTINGS?

The FDA product code for TEMP. SENSOR W/22MM FITTINGS is KPD.

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.

Other records listing Bd Becton Dickinson Vacutainer Systems Preanalytic 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.

View all 632 devices →

Related Devices (Code: KPD)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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