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FDA 510(k)

STER INHAL SOLUT PREFIL BTL W/ADJUST ENTRAIN NEBUL

K-Number: K901301 · 1990-05-31

ApplicantAutomatic Liquid Packaging, Inc.
Decision Date1990-05-31
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

STER INHAL SOLUT PREFIL BTL W/ADJUST ENTRAIN NEBUL is the device name listed in this FDA 510(k) record. The listed applicant is Automatic Liquid Packaging, Inc.. It received FDA 510(k) clearance on 1990-05-31 under 510(k) number K901301. 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 STER INHAL SOLUT PREFIL BTL W/ADJUST ENTRAIN NEBUL?

STER INHAL SOLUT PREFIL BTL W/ADJUST ENTRAIN NEBUL is a medical device that received FDA 510(k) clearance on 1990-05-31. The listed applicant is Automatic Liquid Packaging, Inc.. The 510(k) number is K901301.

When did STER INHAL SOLUT PREFIL BTL W/ADJUST ENTRAIN NEBUL receive FDA 510(k) clearance?

STER INHAL SOLUT PREFIL BTL W/ADJUST ENTRAIN NEBUL received FDA 510(k) clearance on 1990-05-31, under 510(k) number K901301.

Who is the listed applicant for STER INHAL SOLUT PREFIL BTL W/ADJUST ENTRAIN NEBUL?

The FDA 510(k) record lists Automatic Liquid Packaging, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STER INHAL SOLUT PREFIL BTL W/ADJUST ENTRAIN NEBUL?

The FDA product code for STER INHAL SOLUT PREFIL BTL W/ADJUST ENTRAIN NEBUL is CAF.

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Other records listing Automatic Liquid Packaging, Inc. as applicant

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Related Devices (Code: 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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