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FDA 510(k)

SPRINT S-2 INSTRU. CENTER (MODEL 92329)

K-Number: K770129 · 1977-01-28

ApplicantChemetron Health Systems
Decision Date1977-01-28
Product CodeEBW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SPRINT S-2 INSTRU. CENTER (MODEL 92329) is the device name listed in this FDA 510(k) record. The listed applicant is Chemetron Health Systems. It received FDA 510(k) clearance on 1977-01-28 under 510(k) number K770129. The device is classified under product code EBW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPRINT S-2 INSTRU. CENTER (MODEL 92329)?

SPRINT S-2 INSTRU. CENTER (MODEL 92329) is a medical device that received FDA 510(k) clearance on 1977-01-28. The listed applicant is Chemetron Health Systems. The 510(k) number is K770129.

When did SPRINT S-2 INSTRU. CENTER (MODEL 92329) receive FDA 510(k) clearance?

SPRINT S-2 INSTRU. CENTER (MODEL 92329) received FDA 510(k) clearance on 1977-01-28, under 510(k) number K770129.

Who is the listed applicant for SPRINT S-2 INSTRU. CENTER (MODEL 92329)?

The FDA 510(k) record lists Chemetron Health Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPRINT S-2 INSTRU. CENTER (MODEL 92329)?

The FDA product code for SPRINT S-2 INSTRU. CENTER (MODEL 92329) is EBW.

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 Chemetron Health Systems 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.

K760228ANESTHESIA MACHINE, CHEMETRON

Related Devices (Code: EBW)

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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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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