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FDA 510(k)

FILTERED VACUUM SAFETY TRAP BOTTLE

K-Number: K855074 · 1986-03-13

ApplicantBoehringer Laboratories
Decision Date1986-03-13
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FILTERED VACUUM SAFETY TRAP BOTTLE is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Laboratories. It received FDA 510(k) clearance on 1986-03-13 under 510(k) number K855074. The device is classified under product code KDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FILTERED VACUUM SAFETY TRAP BOTTLE?

FILTERED VACUUM SAFETY TRAP BOTTLE is a medical device that received FDA 510(k) clearance on 1986-03-13. The listed applicant is Boehringer Laboratories. The 510(k) number is K855074.

When did FILTERED VACUUM SAFETY TRAP BOTTLE receive FDA 510(k) clearance?

FILTERED VACUUM SAFETY TRAP BOTTLE received FDA 510(k) clearance on 1986-03-13, under 510(k) number K855074.

Who is the listed applicant for FILTERED VACUUM SAFETY TRAP BOTTLE?

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

What is the FDA product code for FILTERED VACUUM SAFETY TRAP BOTTLE?

The FDA product code for FILTERED VACUUM SAFETY TRAP BOTTLE is KDQ.

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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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