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)

BED PADS: D-12 AND D-8

K-Number: K781404 · 1978-09-07

Decision Date1978-09-07
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BED PADS: D-12 AND D-8 is the device name listed in this FDA 510(k) record. The listed applicant is Grant Airmass Corp.. It received FDA 510(k) clearance on 1978-09-07 under 510(k) number K781404. The device is classified under product code FNM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BED PADS: D-12 AND D-8?

BED PADS: D-12 AND D-8 is a medical device that received FDA 510(k) clearance on 1978-09-07. The listed applicant is Grant Airmass Corp.. The 510(k) number is K781404.

When did BED PADS: D-12 AND D-8 receive FDA 510(k) clearance?

BED PADS: D-12 AND D-8 received FDA 510(k) clearance on 1978-09-07, under 510(k) number K781404.

Who is the listed applicant for BED PADS: D-12 AND D-8?

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

What is the FDA product code for BED PADS: D-12 AND D-8?

The FDA product code for BED PADS: D-12 AND D-8 is FNM.

Related Devices (Code: FNM)

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.

↑