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FDA 510(k)

BKS-42 DISPOSABLE VACUUM TUBING PACK

K-Number: K864065 · 1986-12-15

ApplicantAllergan, Inc.
Decision Date1986-12-15
Product CodeHNO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BKS-42 DISPOSABLE VACUUM TUBING PACK is the device name listed in this FDA 510(k) record. The listed applicant is Allergan, Inc.. It received FDA 510(k) clearance on 1986-12-15 under 510(k) number K864065. The device is classified under product code HNO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BKS-42 DISPOSABLE VACUUM TUBING PACK?

BKS-42 DISPOSABLE VACUUM TUBING PACK is a medical device that received FDA 510(k) clearance on 1986-12-15. The listed applicant is Allergan, Inc.. The 510(k) number is K864065.

When did BKS-42 DISPOSABLE VACUUM TUBING PACK receive FDA 510(k) clearance?

BKS-42 DISPOSABLE VACUUM TUBING PACK received FDA 510(k) clearance on 1986-12-15, under 510(k) number K864065.

Who is the listed applicant for BKS-42 DISPOSABLE VACUUM TUBING PACK?

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

What is the FDA product code for BKS-42 DISPOSABLE VACUUM TUBING PACK?

The FDA product code for BKS-42 DISPOSABLE VACUUM TUBING PACK is HNO.

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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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