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FDA 510(k)

P.D. CRADLE

K-Number: K811657 · 1981-07-01

ApplicantLung Care, Inc.
Decision Date1981-07-01
Product Code
DecisionSubstantially Equivalent

Device Summary

P.D. CRADLE is the device name listed in this FDA 510(k) record. The listed applicant is Lung Care, Inc.. It received FDA 510(k) clearance on 1981-07-01 under 510(k) number K811657. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P.D. CRADLE?

P.D. CRADLE is a medical device that received FDA 510(k) clearance on 1981-07-01. The listed applicant is Lung Care, Inc.. The 510(k) number is K811657.

When did P.D. CRADLE receive FDA 510(k) clearance?

P.D. CRADLE received FDA 510(k) clearance on 1981-07-01, under 510(k) number K811657.

Who is the listed applicant for P.D. CRADLE?

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

Related Clinical Trials

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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