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FDA 510(k)

PRESSURE MONITOR MANOMETRIC SYS.

K-Number: K771265 · 1977-11-22

ApplicantPhysio-Control Corp.
Decision Date1977-11-22
Product CodeKLA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PRESSURE MONITOR MANOMETRIC SYS. is the device name listed in this FDA 510(k) record. The listed applicant is Physio-Control Corp.. It received FDA 510(k) clearance on 1977-11-22 under 510(k) number K771265. The device is classified under product code KLA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSURE MONITOR MANOMETRIC SYS.?

PRESSURE MONITOR MANOMETRIC SYS. is a medical device that received FDA 510(k) clearance on 1977-11-22. The listed applicant is Physio-Control Corp.. The 510(k) number is K771265.

When did PRESSURE MONITOR MANOMETRIC SYS. receive FDA 510(k) clearance?

PRESSURE MONITOR MANOMETRIC SYS. received FDA 510(k) clearance on 1977-11-22, under 510(k) number K771265.

Who is the listed applicant for PRESSURE MONITOR MANOMETRIC SYS.?

The FDA 510(k) record lists Physio-Control Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRESSURE MONITOR MANOMETRIC SYS.?

The FDA product code for PRESSURE MONITOR MANOMETRIC SYS. is KLA.

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Other records listing Physio-Control Corp. as applicant

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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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