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FDA 510(k)

FILTER, I.V., WITH FLASH BULB (#4701)

K-Number: K760111 · 1976-07-16

Decision Date1976-07-16
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FILTER, I.V., WITH FLASH BULB (#4701) is the device name listed in this FDA 510(k) record. The listed applicant is Jelco Laboratories. It received FDA 510(k) clearance on 1976-07-16 under 510(k) number K760111. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FILTER, I.V., WITH FLASH BULB (#4701)?

FILTER, I.V., WITH FLASH BULB (#4701) is a medical device that received FDA 510(k) clearance on 1976-07-16. The listed applicant is Jelco Laboratories. The 510(k) number is K760111.

When did FILTER, I.V., WITH FLASH BULB (#4701) receive FDA 510(k) clearance?

FILTER, I.V., WITH FLASH BULB (#4701) received FDA 510(k) clearance on 1976-07-16, under 510(k) number K760111.

Who is the listed applicant for FILTER, I.V., WITH FLASH BULB (#4701)?

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

What is the FDA product code for FILTER, I.V., WITH FLASH BULB (#4701)?

The FDA product code for FILTER, I.V., WITH FLASH BULB (#4701) is FPA.

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 Jelco Laboratories 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 26 devices →

Related Devices (Code: FPA)

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

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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