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FDA 510(k)

DRYDEN INFLATABLE MASK

K-Number: K842472 · 1984-07-06

ApplicantDryden Corp.
Decision Date1984-07-06
Product CodeBSJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DRYDEN INFLATABLE MASK is the device name listed in this FDA 510(k) record. The listed applicant is Dryden Corp.. It received FDA 510(k) clearance on 1984-07-06 under 510(k) number K842472. The device is classified under product code BSJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRYDEN INFLATABLE MASK?

DRYDEN INFLATABLE MASK is a medical device that received FDA 510(k) clearance on 1984-07-06. The listed applicant is Dryden Corp.. The 510(k) number is K842472.

When did DRYDEN INFLATABLE MASK receive FDA 510(k) clearance?

DRYDEN INFLATABLE MASK received FDA 510(k) clearance on 1984-07-06, under 510(k) number K842472.

Who is the listed applicant for DRYDEN INFLATABLE MASK?

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

What is the FDA product code for DRYDEN INFLATABLE MASK?

The FDA product code for DRYDEN INFLATABLE MASK is BSJ.

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.

Other records listing Dryden 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.

View all 21 devices →

Related Devices (Code: BSJ)

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.

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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