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FDA 510(k)

PC-30 PULMONARY COMPUTER

K-Number: K770532 · 1977-04-05

ApplicantCavitron Corp.
Decision Date1977-04-05
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PC-30 PULMONARY COMPUTER is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Corp.. It received FDA 510(k) clearance on 1977-04-05 under 510(k) number K770532. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PC-30 PULMONARY COMPUTER?

PC-30 PULMONARY COMPUTER is a medical device that received FDA 510(k) clearance on 1977-04-05. The listed applicant is Cavitron Corp.. The 510(k) number is K770532.

When did PC-30 PULMONARY COMPUTER receive FDA 510(k) clearance?

PC-30 PULMONARY COMPUTER received FDA 510(k) clearance on 1977-04-05, under 510(k) number K770532.

Who is the listed applicant for PC-30 PULMONARY COMPUTER?

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

What is the FDA product code for PC-30 PULMONARY COMPUTER?

The FDA product code for PC-30 PULMONARY COMPUTER is BZC.

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Other records listing Cavitron Corp. 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.

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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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