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FDA 510(k)

DIASCOPE 2

K-Number: K820745 · 1982-04-01

ApplicantPuritan Bennett Corp.
Decision Date1982-04-01
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DIASCOPE 2 is the device name listed in this FDA 510(k) record. The listed applicant is Puritan Bennett Corp.. It received FDA 510(k) clearance on 1982-04-01 under 510(k) number K820745. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIASCOPE 2?

DIASCOPE 2 is a medical device that received FDA 510(k) clearance on 1982-04-01. The listed applicant is Puritan Bennett Corp.. The 510(k) number is K820745.

When did DIASCOPE 2 receive FDA 510(k) clearance?

DIASCOPE 2 received FDA 510(k) clearance on 1982-04-01, under 510(k) number K820745.

Who is the listed applicant for DIASCOPE 2?

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

What is the FDA product code for DIASCOPE 2?

The FDA product code for DIASCOPE 2 is DRT.

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Other records listing Puritan Bennett Corp. as applicant

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Related Devices (Code: DRT)

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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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