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FDA 510(k)

MANIFOLD & NEBU. FOR SINGLE LINE MACH.

K-Number: K772071 · 1977-11-15

ApplicantInspiron Corp.
Decision Date1977-11-15
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MANIFOLD & NEBU. FOR SINGLE LINE MACH. is the device name listed in this FDA 510(k) record. The listed applicant is Inspiron Corp.. It received FDA 510(k) clearance on 1977-11-15 under 510(k) number K772071. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANIFOLD & NEBU. FOR SINGLE LINE MACH.?

MANIFOLD & NEBU. FOR SINGLE LINE MACH. is a medical device that received FDA 510(k) clearance on 1977-11-15. The listed applicant is Inspiron Corp.. The 510(k) number is K772071.

When did MANIFOLD & NEBU. FOR SINGLE LINE MACH. receive FDA 510(k) clearance?

MANIFOLD & NEBU. FOR SINGLE LINE MACH. received FDA 510(k) clearance on 1977-11-15, under 510(k) number K772071.

Who is the listed applicant for MANIFOLD & NEBU. FOR SINGLE LINE MACH.?

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

What is the FDA product code for MANIFOLD & NEBU. FOR SINGLE LINE MACH.?

The FDA product code for MANIFOLD & NEBU. FOR SINGLE LINE MACH. is CAF.

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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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