Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

INTERSORB DRY BURN VEST & PANTS

K-Number: K822047 · 1982-07-28

Decision Date1982-07-28
Product CodeNAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INTERSORB DRY BURN VEST & PANTS is the device name listed in this FDA 510(k) record. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. It received FDA 510(k) clearance on 1982-07-28 under 510(k) number K822047. The device is classified under product code NAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERSORB DRY BURN VEST & PANTS?

INTERSORB DRY BURN VEST & PANTS is a medical device that received FDA 510(k) clearance on 1982-07-28. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. The 510(k) number is K822047.

When did INTERSORB DRY BURN VEST & PANTS receive FDA 510(k) clearance?

INTERSORB DRY BURN VEST & PANTS received FDA 510(k) clearance on 1982-07-28, under 510(k) number K822047.

Who is the listed applicant for INTERSORB DRY BURN VEST & PANTS?

The FDA 510(k) record lists Chesebrough-Pond'S U.S.A. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERSORB DRY BURN VEST & PANTS?

The FDA product code for INTERSORB DRY BURN VEST & PANTS is NAB.

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 Chesebrough-Pond'S U.S.A. Co. 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 33 devices →

Related Devices (Code: NAB)

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.

↑