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FDA 510(k)

BOTTLE, CONDENSATE (#1628)

K-Number: K760082 · 1976-07-16

ApplicantInspiron Corp.
Decision Date1976-07-16
Product CodeCBC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BOTTLE, CONDENSATE (#1628) is the device name listed in this FDA 510(k) record. The listed applicant is Inspiron Corp.. It received FDA 510(k) clearance on 1976-07-16 under 510(k) number K760082. The device is classified under product code CBC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOTTLE, CONDENSATE (#1628)?

BOTTLE, CONDENSATE (#1628) is a medical device that received FDA 510(k) clearance on 1976-07-16. The listed applicant is Inspiron Corp.. The 510(k) number is K760082.

When did BOTTLE, CONDENSATE (#1628) receive FDA 510(k) clearance?

BOTTLE, CONDENSATE (#1628) received FDA 510(k) clearance on 1976-07-16, under 510(k) number K760082.

Who is the listed applicant for BOTTLE, CONDENSATE (#1628)?

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

What is the FDA product code for BOTTLE, CONDENSATE (#1628)?

The FDA product code for BOTTLE, CONDENSATE (#1628) is CBC.

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Other records listing Inspiron 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.

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Related Devices (Code: CBC)

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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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