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FDA 510(k)

ANESTHESIA/RESPIRATORY DISCONNECT -

K-Number: K831650 · 1983-09-12

ApplicantPlasmedics, Inc.
Decision Date1983-09-12
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA/RESPIRATORY DISCONNECT - is the device name listed in this FDA 510(k) record. The listed applicant is Plasmedics, Inc.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K831650. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANESTHESIA/RESPIRATORY DISCONNECT -?

ANESTHESIA/RESPIRATORY DISCONNECT - is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Plasmedics, Inc.. The 510(k) number is K831650.

When did ANESTHESIA/RESPIRATORY DISCONNECT - receive FDA 510(k) clearance?

ANESTHESIA/RESPIRATORY DISCONNECT - received FDA 510(k) clearance on 1983-09-12, under 510(k) number K831650.

Who is the listed applicant for ANESTHESIA/RESPIRATORY DISCONNECT -?

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

What is the FDA product code for ANESTHESIA/RESPIRATORY DISCONNECT -?

The FDA product code for ANESTHESIA/RESPIRATORY DISCONNECT - is BZQ.

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Other records listing Plasmedics, 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.

K853559STERILE BIOPSY NEEDLESK850263PEDIATRIC ANESTHESIA MASK W/PACIFIER/RING ASSEMBLYK831601APNEA ALARM FOR ADULT-PEDIATRIC & NEONK830604WEDGE PRESSURE CATHETERK823351CENTRAL VENOUS CATHETER

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Official Source

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