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FDA 510(k)

SEARLE NEONATAL OXYGEN PROBE

K-Number: K780850 · 1978-08-23

ApplicantWill Ross Co.
Decision Date1978-08-23
Product CodeCCE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SEARLE NEONATAL OXYGEN PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Will Ross Co.. It received FDA 510(k) clearance on 1978-08-23 under 510(k) number K780850. The device is classified under product code CCE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEARLE NEONATAL OXYGEN PROBE?

SEARLE NEONATAL OXYGEN PROBE is a medical device that received FDA 510(k) clearance on 1978-08-23. The listed applicant is Will Ross Co.. The 510(k) number is K780850.

When did SEARLE NEONATAL OXYGEN PROBE receive FDA 510(k) clearance?

SEARLE NEONATAL OXYGEN PROBE received FDA 510(k) clearance on 1978-08-23, under 510(k) number K780850.

Who is the listed applicant for SEARLE NEONATAL OXYGEN PROBE?

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

What is the FDA product code for SEARLE NEONATAL OXYGEN PROBE?

The FDA product code for SEARLE NEONATAL OXYGEN PROBE is CCE.

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Other records listing Will Ross Co. 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.

K771561DOVER URINE METERK771132KENWOOD BIOLOGICAL STEOILIZ. INDICATORK770608WALKING AIDK770609TABLE, MASSAGE & TREATMHNT, FIXED HEIGHTK770607TRACTION HARNESSK770611PARALLEL BARS

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Related Devices (Code: CCE)

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.

K935778VIA 1-01 INFUSION PUMP/BLOOD CHEMISTRY SYSTEMVia Medical Corp.K912145SYSTEM ATHENA-PRODUCT ENHANCEMENTS, ANESTHESIAS & W Medico TeknikK910453TOPS NEEDLE TIP PROBE & PVC TIP PROBEBaxter Healthcare CorpK905397PB3200 INTRA-ARTERIAL BLOOD GAS MONITORING SYSTEMPuritan Bennett Corp.K896311OPTEX BLOOD GAS MONITORING SYSTEMOptex BiomedicalK890624TISSUE OXYGEN MONITOR SYSTEM, MODEL IIBaxter Healthcare 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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