FDA 510(k)

DETECTOR, BUBBLE & FOAM

K-Number: K780582 · 1978-06-22

Decision Date1978-06-22

Product CodeFJF

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

DETECTOR, BUBBLE & FOAM is the device name listed in this FDA 510(k) record. The listed applicant is Hospal Medical Corp.. It received FDA 510(k) clearance on 1978-06-22 under 510(k) number K780582. The device is classified under product code FJF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DETECTOR, BUBBLE & FOAM?

DETECTOR, BUBBLE & FOAM is a medical device that received FDA 510(k) clearance on 1978-06-22. The listed applicant is Hospal Medical Corp.. The 510(k) number is K780582.

When did DETECTOR, BUBBLE & FOAM receive FDA 510(k) clearance?

DETECTOR, BUBBLE & FOAM received FDA 510(k) clearance on 1978-06-22, under 510(k) number K780582.

Who is the listed applicant for DETECTOR, BUBBLE & FOAM?

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

What is the FDA product code for DETECTOR, BUBBLE & FOAM?

The FDA product code for DETECTOR, BUBBLE & FOAM is FJF.

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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.