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FDA 510(k)

PREFILLED FLEXIBLE R.T. CONTAINERS W/STER. SODIUM

K-Number: K901762 · 1990-07-17

ApplicantAutomatic Liquid Packaging, Inc.
Decision Date1990-07-17
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PREFILLED FLEXIBLE R.T. CONTAINERS W/STER. SODIUM 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 1990-07-17 under 510(k) number K901762. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PREFILLED FLEXIBLE R.T. CONTAINERS W/STER. SODIUM?

PREFILLED FLEXIBLE R.T. CONTAINERS W/STER. SODIUM is a medical device that received FDA 510(k) clearance on 1990-07-17. The listed applicant is Automatic Liquid Packaging, Inc.. The 510(k) number is K901762.

When did PREFILLED FLEXIBLE R.T. CONTAINERS W/STER. SODIUM receive FDA 510(k) clearance?

PREFILLED FLEXIBLE R.T. CONTAINERS W/STER. SODIUM received FDA 510(k) clearance on 1990-07-17, under 510(k) number K901762.

Who is the listed applicant for PREFILLED FLEXIBLE R.T. CONTAINERS W/STER. SODIUM?

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 PREFILLED FLEXIBLE R.T. CONTAINERS W/STER. SODIUM?

The FDA product code for PREFILLED FLEXIBLE R.T. CONTAINERS W/STER. SODIUM is BTT.

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Other records listing Automatic Liquid Packaging, Inc. 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.

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Related Devices (Code: BTT)

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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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