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FDA 510(k)

RESCAL

K-Number: K781759 · 1978-11-27

Decision Date1978-11-27
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESCAL is the device name listed in this FDA 510(k) record. The listed applicant is Diemolding Corp.. It received FDA 510(k) clearance on 1978-11-27 under 510(k) number K781759. The device is classified under product code BZA. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESCAL?

RESCAL is a medical device that received FDA 510(k) clearance on 1978-11-27. The listed applicant is Diemolding Corp.. The 510(k) number is K781759.

When did RESCAL receive FDA 510(k) clearance?

RESCAL received FDA 510(k) clearance on 1978-11-27, under 510(k) number K781759.

Who is the listed applicant for RESCAL?

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

What is the FDA product code for RESCAL?

The FDA product code for RESCAL is BZA.

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 Diemolding 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 12 devices →

Related Devices (Code: BZA)

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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