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FDA 510(k)

KRYORACK/4

K-Number: K780757 · 1978-06-06

ApplicantStreck Laboratories, Inc.
Decision Date1978-06-06
Product CodeJRR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KRYORACK/4 is the device name listed in this FDA 510(k) record. The listed applicant is Streck Laboratories, Inc.. It received FDA 510(k) clearance on 1978-06-06 under 510(k) number K780757. The device is classified under product code JRR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KRYORACK/4?

KRYORACK/4 is a medical device that received FDA 510(k) clearance on 1978-06-06. The listed applicant is Streck Laboratories, Inc.. The 510(k) number is K780757.

When did KRYORACK/4 receive FDA 510(k) clearance?

KRYORACK/4 received FDA 510(k) clearance on 1978-06-06, under 510(k) number K780757.

Who is the listed applicant for KRYORACK/4?

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

What is the FDA product code for KRYORACK/4?

The FDA product code for KRYORACK/4 is JRR.

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Other records listing Streck Laboratories, Inc. as applicant

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Related Devices (Code: JRR)

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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