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FDA 510(k)

RESPIRATORY SUPPORT SYSTEM, NEONATAL

K-Number: K760340 · 1976-08-11

Decision Date1976-08-11
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESPIRATORY SUPPORT SYSTEM, NEONATAL is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1976-08-11 under 510(k) number K760340. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESPIRATORY SUPPORT SYSTEM, NEONATAL?

RESPIRATORY SUPPORT SYSTEM, NEONATAL is a medical device that received FDA 510(k) clearance on 1976-08-11. The listed applicant is Sherwood Medical Industries. The 510(k) number is K760340.

When did RESPIRATORY SUPPORT SYSTEM, NEONATAL receive FDA 510(k) clearance?

RESPIRATORY SUPPORT SYSTEM, NEONATAL received FDA 510(k) clearance on 1976-08-11, under 510(k) number K760340.

Who is the listed applicant for RESPIRATORY SUPPORT SYSTEM, NEONATAL?

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

What is the FDA product code for RESPIRATORY SUPPORT SYSTEM, NEONATAL?

The FDA product code for RESPIRATORY SUPPORT SYSTEM, NEONATAL is BZQ.

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 Sherwood 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.

View all 62 devices →

Related Devices (Code: BZQ)

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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